Caraga Regional Hospital Tender

Description Republic Of The Philippines Department Of Health Caraga Regional Hospital Surigao City Bids And Awards Committee Ooooooo ----------------------------------------------------------------------------------------------------------------------------- @@@@@@@@@@@@@@@@@@@@@@@@@@@@@@@@@@@@@@@@@@@@@@@@@@@@ Invitation To Bid Ib No. 2024-11-26 (89) Supply And Delivery Of Various Cardio-diagnostic Medical Equipment - Rebid Abc: ₱ 1,700,000.00 ================================================================= 1. The Caraga Regional Hospital (crh), Through The General Appropriation Act (gaa), Hfep - Saa No. 2024-02-0271 Intends To Apply The Sum Of Being The Approved Budget For The Contract (abc) Of One Million Seven Hundred Thousand Pesos Only ( Php 1,700,000.00) Under The Contract For The Supply And Delivery Of Various Cardio-diagnostic Medical Equipment - Rebid. Bids Received In Excess Of The Abc Shall Be Automatically Rejected At Bid Opening And Items Below Are Subject For A Competitive Bidding, To Wit: Item No. Description Quantity Unit Of Measure Unit Cost Total Cost 1 Portable Pulse Oximeter, Heavy Duty Rechargeable W/ Finger Prongs For Neonate, Pedia, Adult Size 4 Set 50,000.00 200,000.00 2 Cardiac Defibrillator 1 Unit 1,500,000.00 1,500,000.00 Grand Total ₱ 1,700.00.00 Technical Specifications 1. Portable Pulse Oximeter, Heavy Duty Rechargeable W/ Finger Prongs For Neonate, Pedia, Adult Size Description Patient Category Pulse Oximeter Reading For Oxygen Saturation Level Between 95% And 100%. If You Have A Lung Disease Such As Copd Or Pneumonia, Your Normal Oxygen Saturation Level May Be Lower. Purpose Of Use Clinical Department / Ward: Ambulatory Surgery Unit Technical Specifications Enclosure: For People: Pedia, Adult & Neonate Alarms: Yes Categories: Patient Status And System Status Notification: Audible And Visual Setting: Full Storage, Low Battery And Sensor Off Range: Pulse Rate (25-350 Bpm), Spo2 (0-100%) Alarm Volume: Within Range Level 0-85 Db Range, Accuracy And Resolution: Range Type: Range Values Measurement Ranges: Spo2 Measuring Range: 0-100% Pulse Rate: Range 25-350 Bpm Measurement Accuracy: Spo2 Measuring Accuracy: 70-100% (±2%), <70% Undefined Pulse Rate Measuring Accuracy: ±2bpm/±2% Take Maximum Resolution Spo2: 1% Pulse Rate: 1 Bpm Electrical Ac Power Requirement 100-240va, 50-60hz Power Consumption: 20va Maximum Batteries Types: Alkaline/ni-mh Aa Or Aaa 1.5v Rechargeable Batteries, Iec: Lr6 Operating Time: ≥20hours Charge Time: ≤ 6hours Environment Operating Temperature: 0-45ºcelsius Storage Temperature-20-60ºcelsius Operating Humidity30-95% Operating Altitude: -500-5000m (optional) Trends Types: Tabular Memory: Save Total 120 Hours Data Events. Save Data And Time, Alarm Conditions, Pulse Rate And Spo2 Measurements Features: • Suitable For Adult, Pediatric, Neonatal Patients. • High Resolution 2.8inches Color Lcd Display. • Three Selectable Working Modes: Spot Check, Continuous Monitoring And Recording. • Adjustable Audible And Visual Alarms. • Patient Information Management. • Trend Data Can Be Transfer To Your Pc To Record, Analyze, Report And Archive. • Batteries To Support Up To 20 Hours Continuous Working. • Protective Cover And Carrying Case Perfect For Portable Monitoring Needs. Technical Services As Follows: • System Warranty Must Be Five (5) Years • Calibration Of The Unit Must Be Performed After Installation With Certificate • Service Call Within 24 Hours Maximum • Supplier Must Deliver And Install The Unit Without Cost To The Owner • Training Of End-users And Biomed Engineer Must Be Done On-site With Minimum Of 1 Day Period. Physical/chemical Characteristics • The Oximeter Utilizes An Electronic Processor And A Pair Of Small Light-emitting Diodes (leds) Facing A Photodiode Through A Translucent Part Of The Patient's Body, Usually A Fingertip Or An Earlobe. Accessories, Consumables, Spare Parts, Other Components • Dc 3v (6x 1.5v Aaa Batteries Rechargeable) • 1 Set Pedia Fingertip Censor Oximeter Probe • 1 Set Adult Fingertip Censor Oximeter Probe • 1 Set Neonate Fingertip Censor Oximeter Probe Training, Installation And Utilisation Pre-installation Requirements Supplier To Perform Installation, Safety And Operation Checks Before Handover. Requirements For Commissioning Local Clinical Staff To Affirm Completion Of Installation Training Of User/s Training Of Users And Biomed Engineer & Staff In Operation And Basic Maintenance Shall Be Provided User Care To Demonstrate The Proper Cleaning And Disinfection With Provision Of Printed Cards Or Tags Beside The Unit. Warranty And Maintenance Warranty 5 Years Environmental Factors • Capable Of Being Stored Continuously In Ambient Temperature Of 0 To 50 Deg Celsius And Relative Humidity Of 15 To 90%. • Capable Of Operating Continuously In Ambient Temperature Of 10 To 40 Deg Celsius And Relative Humidity Of 15 To 90% Documentation Documentation Requirements User, Technical And Maintenance Manuals To Be Supplied In English Language. Service Manual In English. List To Be Provided Of Important Spares And Accessories, With Their Part Serial Numbers And Cost. Certificate Of Calibration, Warranty And Inspection To Be Provided By Supplier. Safety And Standards International Standards En 12470-5: European Standard For Clinical Thermometer Performance - Infrared Ear Thermometers Astm E1965-1998: Astm (american Society Of Testing And Methodology) - Standard Specification Of Infrared Thermometers For Intermittent Determination Of Patient Temperature En 980: Graphical Symbols For Use In The Labeling Of Medical Devices En 1041: Information Supplied By The Manufacturer With Medical Devices En 60601-1: Medical Electrical Equipment Part 1: General Requirements For Safety (iec: 60601-1:1998) En 60601-1-2: Medical Electrical Equipment Part 1-2: General Requirements For Safety - Collateral Standard: Electromagnetic Compatibility - Requirements And Test (iec 60601-1-2:2001) Delivery Period 45 Calendar Days From Receipt Of The Notice To Proceed Terms Of Payment Upon Full Delivery, Installed, Tested And Commissioned Post-qualification Must Be Willing To Send Demo Unit To Caraga Regional Hospital And/or Site Visit To Nearest Hospital. Supplier To Provide Actual Prototype/demo-unit During The Conduct Of Post Qualification- Same Brand & Model Of Offered Bid, No Alteration Of Actual Submitted Brochure Technical Specification Sheets. Failure To Comply With The Preferred Schedule Of The Procuring Entity For The Post Qualification Can Be A Ground For Disqualification. (no Extensions Allowed.) Other Terms And Conditions Of Acceptability: Supplier Must Comply With The Following Conditions: 1. Must Be The Authorized Distributor Of The Principal Company Of The Equipment And The Necessary Consumables In The Philippines 2. Submit Certificate Of Training Of The Company Engineer /technical Personnel And Product Specialist Issued By The Principal Or Manufacturer 3. Provide Company Response Within 24-48hrs In Case Technical Problems Or Equipment Breakdown 4. Must Submit Notarized Certificate Of Availability Of Spare Parts For The Next 5years 5. Supplier Must Have An Actual Installation Of The Offered Brand And Model 6. Provision On-site Training For End-user & Maintenance Personnel On Basic Preventive Maintenance And Proper Operation Of The Unit. 2. Cardiac Defibrillator Description Defibrillator Is Required For Reviving The Heart Functions By Providing Selected Quantum Of Electrical Shocks With Facility For Monitoring Vital Parameters. Purpose Of Use Clinical Or Other Purpose Defibrillator Is Used To Prevent Or Correct An Arrhythmia, An Uneven Heartbeat That Is Too Slow Or Too Fast. Clinical Department/ward Ambulatory Surgical Unit Overview Of Functional Requirements A Defibrillator Is A Device Intended To Treat Pulseless Ventricular Fibrillation Or Pulseless Ventricular Tachycardia. To Do This, The Defibrillator Passes A Brief Electrical Current Through The Heart, Which Depolarizes Cardiac Muscle And Allows The Body’s Natural Pacemaker To Re-establish A Proper Rhythm. A Pair Of Electrodes, Along With Electrically Conductive Gel, Facilitates This Current Via A Difference In Potential (or Voltage); The Gel Reduces The Natural Resistivity Of Body Tissues And Prevents Electrical Burn. Technical Characteristics Detailed Requirements 1. Defibrillation Monitors Can Monitor Ecg, Resp, Spo2, Nibp, Heart Rate And Pulse Rate Etc. Vital Sign Parameters. This Product Is Suitable For Manual Defibrillation, Aed Defibrillation, Pacing And Vital Signs Monitoring. 2. Should Be A Low Energy Biphasic Defibrillator Monitor With Recorder, Having Capability To Deliver Shocks From 2 Joules To 360 Joules. 3. Should Monitor Ecg Through Paddles, Pads And Monitoring Electrodes And Defibrillate Through Pads And Paddles. 4. Should Compensate For Body Impedance For A Range Of 25 To 150 Ohms 5. Should Have A Built In 50 Mm Strip Printer 6. Should Have High Resolution More Than 8 Inch Color Display For Viewing Monitoring Parameters Like Ecg, Spo2, Nibp, Heart Rate And Pulse Rate With 4 Waveform Capability Of 4 Seconds. 7. Both Adult And Pediatric Paddles Should Be Available. 8. Should Have Event Summary Facility For Recording And Printing At Least 55 Events. 9. Should Have A Battery Capable Of Usage For At Least 5 Hours Of Monitoring. 10. Should Be Capable Of Printing Reports On Event Summary, Configuration, Self-test, Battery Capacity Etc. 11. Should Have Facility For Self-test/check Before Usage And Set Up Function. 12. Should Have Facility To Monitor Parameters Like Spo2, Nibp, Heart Rate And Pulse Rate Along With Noninvasive Pacing (demand & Fixed Mode) Facility. 13. Should Be Able To Upgrade The Defibrillator For 12 Lead Ecg Monitoring And Ecg Transmission. 14. Pacing Method: Rectangular Wave 15. Pulse Width: 22 Msec 16. Pacing Rate: 0-180 Ppm 17. Output Current: 150 Ma Max 18. External Output:usb 19. Manual Defibrillation Modes Include Synchronous Cardioversion And Asynchronous Defibrillation 20. Having On-demand Pacing And Fixed Pacing Mode, For Patients With Cardiac Arrest And Acute Severe Slow Arrhythmia, Invitro Non-invasive Pacing Mode Is Rapid, Easy To Master, Time-saving And Improve Recovery Success Rate. 21. With The Protection Of Ip44, S5 Offers Reliable Performance In A Variety Of Adverse Conditions. 22. Power Input To Be 120-240vac, 50-60 Hz Should Have A Battery Capable Of Usage For Least Five Hours. 23. Ups Features: • 1500va/ 1000w Capacity • Built In Avr Function • Lcd Interface For Easy Configuration • One Hour Operation In The Event Of Mains Power Failure. • At Least 4 Outlets Physical/chemical Characteristics • An Aed Is A Lightweight, Battery-operated, Portable Device That Checks The Heart's Rhythm And Sends A Shock To The Heart To Restore Normal Rhythm. The Device Is Used To Help People Having Cardiac Arrest. Sticky Pads With Sensors, Called Electrodes, Are Attached To The Chest Of Someone Who Is Having Cardiac Arrest. Environmental Factors - Operating Conditions: 0°celsius - 50°celsius / 10 % – 95% Rh. - Storage Conditions: -10°celsius - 50°celsius / 10% – 95% Rh. - Atmospheric Pressure Up To 700 Hpa (altitude Of 3,000m). - Ingress Protection Rating: Ip44. Accessories, Consumables, Spare Parts, Other Components • Defibrillator With Aed And External Pacemaker – 1 Set • Adult With Built In Pediatric External Paddles – 1 Set • Patient Cables – 1 Set • Ecg Rolls (80mm X 20 M) – 50 Rolls • Adult And Pedia Spo2 Reusable Sensor – 1 Set Each • Adult And Pedia Nibp Cuff And Hose – 1 Set Each • 1 Box Aed Multifunction Pads For Adults And Pedia - 10 Pairs With Each Unit • 2x Sets Of Spare Batteries, Packed Separately. • With Trolley And Caster Wheels Training, Installation And Utilization Pre-installation Requirements (if Relevant) • The Supplier To Perform Installation, Safety Of The Machine And Operation Checks Before Handover Local Clinical Staff To Affirm Completion Of Installation • Calibration Certificate, C.e, Iso • Training Of User And Biomed In Operation And Basic Maintenance Shall Be Provided • Unit To Be Cleanable With Alcohol Or Wipes. Supplier Will Install Instruction Tags To Be Placed In The Machine Equipment On The Basic Operation And Maintenance And Care. Requirements For Commissioning • Calibration Certificate • Warranty Certificate Training Of Users (if Relevant) Training Of Users And Biomed In Operation And Basic Maintenance Shall Be Provided User Care (if Relevant) Unit To Be Cleanable With Alcohol Or Chlorine Wipes Supplier Will Install Instruction Tags To Be Placed In The Machine Cart/ Trolley On The Basic Operation, Maintenance And Care Warranty And Maintenance - Preventive Maintenance Upon Covered Of Warranty • 5 Years Parts And Labor * Cleaning And Maintenance Of The Machine * Shall Have Spare Parts Availability Once The End User Needs It Safety And Standard International Standards May Be Certified In At Least One Of The Following: So 13485:2003 Medical Devices -- Quality Management Systems -- Requirements For Regulatory Purposes (australia, Canada And Eu) Iso 14971:2007 Medical Devices -- Application Of Risk Management To Medical Devices Iec 60601-1:2012 Medical Electrical Equipment - Part 1: General Requirements For Basic Safety And Essential Performance Iec 60601-1-1:2000 Medical Electrical Equipment - Part 1-1: General Requirements For Safety - Collateral Standard: Safety Requirements For Medical Electrical Systems Iec 60601-1-2:2007 Medical Electrical Equipment - Part 1-2: General Requirements For Basic Safety And Essential Performance - Collateral Standard: Electromagnetic Compatibility - Requirements And Tests Iec 60601-1-8:2012 Medical Electrical Equipment - Part 1-8: General Requirements For Basic Safety And Essential Performance - Collateral Standard: General Requirements, Tests And Guidance For Alarm Systems In Medical Electrical Equipment And Medical Electrical Systems Iec 60601-2-25:2011 Medical Electrical Equipment - Part 2-25: Particular Requirements For The Basic Safety And Essential Performance Of Electrocardiographs Iec 60601-2-27:2011 Medical Electrical Equipment - Part 2-27: Particular Requirements For The Basic Safety And Essential Performance Of Electrocardiographic Monitoring Equipment Iec 60601-2-49:2011 Medical Electrical Equipment - Part 2-49: Particular Requirements For The Basic Safety And Essential Performance Of Multifunction Patient Monitoring Equipment Iec 60601-2-4:2010+amd1:2018 Csv Consolidated Version Medical Electrical Equipment - Part 2-4: Particular Requirements For The Basic Safety And Essential Performance Of Cardiac Defibrillators. - Iec 60601-1-6:2010 Medical Electrical Equipment - Part 1-6: General Requirements For Basic Safety And Essential Performance - Collateral Standard: Usability. Documentation • Advanced Maintenance Tasks Required Shall Be Documented • User Technical And Maintenance Manuals To Be Supplied In English Language • List To Be Provided Of Equipment And Procedures Required For Local Calibration And Routine Maintenance • Certificate Of Calibration And Inspection To Be Provided • Contact Details Of Manufacturer, Supplier And Local Services To Be Provided Delivery Period • 45 Calendar Days From Receipt Of The Notice To Proceed Terms Of Payment • Upon Full Delivery, Installed, Tested And Commissioned Service Center Must Have Service Center Within Caraga Region, Cebu City, Cdo Or Davao City. Post-qualification Must Be Willing To Send Demo Unit To Caraga Regional Hospital And/or Site Visit To Nearest Hospital. Supplier To Provide Actual Prototype/demo-unit During The Conduct Of Post Qualification- Same Brand & Model Of Offered Bid, No Alteration Of Actual Submitted Brochure Technical Specification Sheets. Failure To Comply With The Preferred Schedule Of The Procuring Entity For The Post Qualification Can Be A Ground For Disqualification. (no Extensions Allowed.) Other Terms And Conditions Of Acceptability: Supplier Must Comply With The Following Conditions: 1. Must Be The Authorized Distributor Of The Principal Company Of The Equipment And The Necessary Consumables In The Philippines 2. Submit Certificate Of Training Of The Company Engineer /technical Personnel And Product Specialist Issued By The Principal Or Manufacturer 3. Provide Company Response Within 24-48hrs In Case Technical Problems Or Equipment Breakdown 4. Must Submit Notarized Certificate Of Availability Of Spare Parts For The Next 5years 5. Supplier Must Have An Actual Installation Of The Offered Brand And Model 6. Provision On-site Training For End-user & Maintenance Personnel On Basic Preventive Maintenance And Proper Operation Of The Unit. This Is A Partial Bid Or Line Item Bid. Technical Specification And Other Terms Of Reference Are Hereby Posted In Philgeps And Form An Integral Part Of This Invitation To Bid. 2. The Crh Now Invites Bids For The Procurement Of The Above-captioned Project. Delivery Of The Goods Is Required Within The Period Specified Under Section Vi (schedule Of Requirements). Bidders Should Have Completed, Within Five (5) Years From The Date Of Submission And Receipt Of Bids, A Contract Similar To The Project. Section 23.4.1.3. (ra 9184) The Bidder Must Have Completed A Single Contract That Is Similar To This Project, Equivalent To At Least Fifty Percent (50%) Of The Abc. Slcc Must Be Within 5 Years From The Submission Of Bids. (based On The Completion Date). Slcc Shall Be The Same Or Similar In Nature. Similar In Nature Means, The Bidder Shall Have An Slcc Of Any Medical Equipment. For Procurement Where The Procuring Entity Has Determined, After The Conduct Of Market Research, That Imposition Of Either (a) Or (b) Will Likely Result To Failure Of Bidding Or Monopoly That Will Defeat The Purpose Of Public Bidding: The Bidder Should Comply With The Following Requirements: A. Completed At Least Two (2) Similar Contracts, The Aggregate Amount Of Which Should Be Equivalent To At Least Fifty Percent (50%) In The Case Of Non-expendable Supplies And Services Or Twenty-five Percent (25%) In The Case Of Expendable Supplies] Of The Abc For This Project; And B. The Largest Of These Similar Contracts Must Be Equivalent To At Least Half Of The Percentage Of The Abc As Required Above. 3. Bidding Will Be Conducted Through Open Competitive Bidding Procedures Using A Nondiscretionary “pass/fail” Criterion As Specified In The 2016 Revised Implementing Rules And Regulations (irr) Of Republic Act (ra) 9184, Otherwise Known As The “government Procurement Reform Act”. Bidding Is Restricted To Filipino Citizens/sole Proprietorships, Partnerships, Or Organizations With At Least Sixty Percent (60%) Interest Or Outstanding Capital Stock Belonging To Citizens Of The Philippines, And To Citizens Or Organizations Of A Country The Laws Or Regulations Of Which Grant Similar Rights Or Privileges To Filipino Citizens, Pursuant To Ra 5183. 4. Interested Bidders May Obtain Further Information From The Bids And Awards Committee (bac) Secretariat, At Procurement Section, Caraga Regional Hospital, Surigao City And Inspect The Bidding Documents At The Address Given Above During 8:00 Am – 5:00 Pm, Monday To Friday. 5. A Complete Set Of Bidding Documents May Be Acquired By Interested Bidders On November 04, 2024 – November 26, 2024 On Or Before 10:00 A.m. From The Address Above And Upon Payment Of The Applicable Fee For The Bidding Documents, Pursuant To The Latest Guidelines Issued By The Gppb, In The Amount Specified Below: Bidding Schedule Pre-bidding Conference November 12, 2024 At 9:00 O’clock In The Morning Via Zoom Platform Link: Join Zoom Meeting Https://us06web.zoom.us/j/81678548186?pwd=4or3dzbrdwqiiv2debcomwvnwawado.1 Meeting Id: 816 7854 8186 Passcode: 537764 Deadline Of Submission Of Bids November 26, 2024 At 10:00 A.m... Via Online And Submit Your Bidding Documents To This Email Address: Crhbac2020@gmail.com . Opening Of Bids November 26, 2024 At 2:00 P.m. Via Zoom Platform. Link: Join Zoom Meeting Https://us06web.zoom.us/j/82377627183?pwd=bktxdbazdepngg2lajuqkbwmgso0xh.1 Meeting Id: 823 7762 7183 Passcode: 543950 Complete Philippine Bidding Documents Please Click The Link Below For The Complete Pbd: Https://drive.google.com/drive/folders/1ajxtsuo4-8c5s18e9_2iuternkrbed6b?usp=sharing Payment Of Bidding Documents Php 5,000.00 It May Also Be Downloaded Free Of Charge From The Website Of The Philippine Government Electronic Procurement System (philgeps) And The Website Of The Procuring Entity, Provided That Bidders Shall Pay The Applicable Fee For The Bidding Documents Not Later Than The Submission Of Their Bids. The Following Philippine Bidding Documents Can Be Accessed In The Philgeps, To Wit: A. Technical Specification / Terms Of Reference/ List Of Items B. Instruction To Bidders: B.1. Documents To Be Submitted (checklist- This Will Be Discussed During The Pre-bid Conference) B.2. Memorandum Of Undertaking – Provision Thereof Is Strictly Implemented C. Guidelines On The Conduct Of The Electronic Submission And Receipt Of Bids By The Procuring Entity – Caraga Regional Hospital (crh) D. Philippine Bidding Documents 6. The Crh Will Hold A Pre-bid Conference On The Above-mentioned Date, Time And Venue, Which Shall Be Opened To Prospective Bidders. The Pre-bidding Conference And Opening Of Bids Shall Be Conducted Through Videoconferencing, Webinar Or Virtual. Please Send Your Intent To Participate To Our Email Address As Provided Below. 7. Bids Must Be Duly Received By The Bac Secretariat At Via Designated Email On Or Before November 26, 2024 At 10:00 O’clock In The Morning. All Bids Must Be Accompanied By A Bid Security In Any Of The Acceptable Forms And In The Amount Stated In Itb Clause 18. Bid Opening Shall Be On November 26, 2024 At 2:00 O’clock In The Afternoon At The Bac Conference Room, Beside Procurement Office, Caraga Regional Hospital, Rizal Street, Surigao City As Virtual / Electronic Bidding. Bids Will Be Opened In The Presence Of The Bidders’ Representatives Who Choose To Attend At The Address Above. Late Bids Shall Not Be Accepted. 8. Furthermore, The Standard Philippine Bidding Document (pbd) Is Form And Part Of This Invitation In Accordance To Ra 9184 And Other Applicable Laws, Rules And Policy. 9. The Crh Reserves The Right To Reject Any And All Bids, Declare A Failure Of Bidding, Or Not Award The Contract At Any Time Prior To Contract Award In Accordance With Section 41 Of Ra 9184 And Its Irr, Without Thereby Incurring Any Liability To The Affected Bidder Or Bidders. 10. The Opening And Receipt Of Bids Is Strictly Implemented Through Electronic Submission. Given The Covid-19 Pandemic, Procurement Activity Has Been Expedient And One Of This Is The Conduct Of Electronic Submission Of Bids. The Crh Thru The Bids And Awards Committee (bac) Has Submitted Certification, Certified By The Highest Official Managing The Information Technology, Describing The Electronic System Or Procedure To Be Used By The Crh For The Electronic Submission And Receipts Of Bids And A Statement That The Same Is Compliant With The Gppb Resolution No. 12-2020 Requirements. 11. Bidding Documents Shall Be Emailed To This Email Address, With Activated Password To: Crhbac2020@gmail.com. You May Deposit On Line For The Payment Of The Bidding Documents To This Account Below: Bank Name: Land Bank Of The Philippines Account Name: Caraga Regional Hospital-trust Fund Account Number: 0982 -1288 – 70 12. Furthermore Deposit Slip Shall Be Submitted Via Email To: Crhprocurement.bac@gmail.com. 13. The Procuring Entity Will No Longer Accept Nor Entertain Any Form Of Bids Submission Except Electronic. Failure To Comply Electronic Submission Will Be Immediately Disqualified. Guideline On The Electronic Submission Is Hereby Attached. 14. Please Fill Up The Caraga Regional Hospital Supplier’s Registry To This Link: Https://bit.ly/crh_suppliersregistry 15. For Further Information, Please Inquire To: Bac Secretariat Caraga Regional Hospital. Rizal Street, Surigao City Tel. Nos. (086) 826-1575 Local 194 (086) 826-9058 Mobile Nos: Globe: 0953-9212-832 / Smart: 0985-0508-783 E-mail Address: Crhprocurement.bac@gmail.com Fb Page: Caraga Regional Hospital – Bids And Awards Committee Approved By: (sgd) Atty. Ma. Flordelin T. Ensomo, Cpa Attorney Iv Chairman, Bids And Awards Committee