Invitation to Bid - Pulse Oximeter (V2) in TIRUVALLUR, TAMIL NADU
Bid Publish Date
19-Feb-2026, 12:39 pm
Bid End Date
19-Mar-2026, 1:00 pm
EMD
₹60,000
Value
₹12,00,000
Location
Progress
Public procurement opportunity for Indian Council Of Medical Research (icmr) Pulse Oximeter (V2) (Q2) ( PAC Only) in TIRUVALLUR, TAMIL NADU. Quantity: 12 issued by. Submission Deadline: 19-03-2026 13: 00: 00. View full details and respond.
Tender Data
Bid Details
Quantity
12
Bid Type
Two Packet Bid
Bid Validity
180 (Days)
Bid Type
Service
Evaluation
Total value wise evaluation
Inspection Required
No
Tech Clarification Time
2 Days
Requirements
Min. Avg. Annual Turnover
6
OEM Avg. Turnover
24
Past Performance
80 %
Experience Required
3 Year (s)
Arbitration Clause
No
Mediation Clause
No
Additional Tender Data
Commercial Details
Tender Category
Goods
Bid To RA
No
Bid To RA Enabled
No
Item Category
Pulse Oximeter (V2) (Q2) ( PAC Only )
Authority Records
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Documents 6
GeM-Bidding-8938467.pdf
Main Document
Other Documents
OTHER
CATALOG-Specification-1
CATALOG Specification
Other Documents
OTHER
Buyer uploaded ATC document
ATC
GEM General Terms and Conditions Document
GEM_GENERAL_TERMS_AND_CONDITIONS
Corrigendum Updates
1 Update Update
Extended Deadline
19-Mar-2026, 7:30 am
Opening Date
19-Mar-2026, 8:00 am
Required Documents
Experience Criteria
Past Performance
Bidder Turnover
Certificate (Requested in ATC)
OEM Authorization Certificate
OEM Annual Turnover
Additional Doc 1 (Requested in ATC)
Additional Doc 2 (Requested in ATC)
Additional Doc 3 (Requested in ATC)
Additional Doc 4 (Requested in ATC)
Compliance of BoQ specification and supporting document *In case any bidder is seeking exemption from Experience / Turnover Criteria
the supporting documents to prove his eligibility for exemption must be uploaded for evaluation by the buyer
Technical Specifications
1 Item
Item #1 Details
View Catalog| Category | Specification | Requirement |
|---|---|---|
| General | Product Description | Pulse Oximeter |
| PRODUCT INFORMATION | Type of Pulse Oximeter | Table Top |
| PRODUCT INFORMATION | Should work during motion and very low perfusion conditions | Yes |
| PRODUCT INFORMATION | Special Signal processing Technology (Motion artifact rejection) | Nellcor |
| PRODUCT INFORMATION | SPO2 probes utility | Reusable |
| PRODUCT INFORMATION | Oxygen saturation Range | 0-100% |
| PRODUCT INFORMATION | Display of SPO2 and PR | Digital display with plethysmograph with trends |
| PRODUCT INFORMATION | Display should be readable from at least 3 feet | Yes |
| PRODUCT INFORMATION | Saturation displayed on the screen | Yes |
| PRODUCT INFORMATION | Pulse Rate displayed on the screen | Yes |
| PRODUCT INFORMATION | Perfusion Index displayed on the screen | Yes |
| PRODUCT INFORMATION | Status of battery charging displayed on the screen | Yes |
| PRODUCT INFORMATION | Sensor off /on status | Yes |
| PRODUCT INFORMATION | Audible and visual Alarms | Yes |
| PRODUCT INFORMATION | Alarm override facility should be present | Yes |
| PRODUCT INFORMATION | Trends in Hours | 96 Or higher |
| PRODUCT INFORMATION | Type of trend display | Graphical |
| PRODUCT INFORMATION | Power source | Inbuilt re-chargeable battery and mains 220-240 V , 50 Hz AC operation |
| PRODUCT INFORMATION | Automatic switch from mains to battery in case of power failure | Yes |
| PRODUCT INFORMATION | Patient extension cable | Yes |
| PRODUCT INFORMATION | Display of Respiratory Rate (RRP) | Yes |
| PROBES | Type of probe | Adult, Pediatric, Neonatal |
| PROBES | Probe usage | Reusable |
| NIBP PARAMETERS | Non invasive blood pressure (NIBP) provided | No |
| NIBP PARAMETERS | Type of BP monitoring | NA (If NIBP not provided) |
| NIBP PARAMETERS | NIBP range in mmHg | NA (If NIBP not provided) |
| NIBP PARAMETERS | Cuff size | NA (If NIBP not provided) |
| NIBP PARAMETERS | Number of cuff's provided | NA(If NIBP not provided) |
| CERTIFICATIONS | Compliance to Medical Device Rules (MDR) 2017 as amended till date | Yes |
| CERTIFICATIONS | Availability of valid Medical Device license for the product issued from the competent authority defined under Drugs and Cosmetic Act 1940 and Rules made there under as amended till date | Yes |
| CERTIFICATIONS | Certification for manufacturing unit | ISO:13485 (Latest) |
| CERTIFICATIONS | Availability of Test Report for each supplied batch/product as per Medical Device Rule (MDR) 2017 as amended till date | Yes |
| WARRANTY | Warranty in Years (Option of comprehensive warranty is available through bidding only, which if opted will supersede normal warranty in the catalogue) | 5 Or higher |