Bid Publish Date
15-Jul-2026, 10:46 am
Bid End Date
25-Jul-2026, 11:00 am
Location
Progress
RATender Overview
The Health Department Andaman & Nicobar seeks procurement of the Transducer Protector (V2) – Q2 category. Scope centers on supply of medical-grade transducer protectors, with emphasis on compliance, batch testing, and regulatory licenses. Key differentiators include adherence to the Medical Device Rules (MDR) 2017, an active Medical Device license, and batch test reports for each supplied unit. The contract contemplates supply-only scope, with advance sample approval and shelf-life verification required prior to delivery. Unique terms include option-based quantity adjustments up to 25% and delivery timing aligned to the last original order date, ensuring uninterrupted procurement for health facilities.
Technical Specifications & Requirements
Product: Transducer Protector (V2) – Q2 category
Certifications: MDR 2017 compliance, Medical Device license under Drugs and Cosmetic Act, Manufacturing unit Certification, batch test reports per MDR
Shelf life: minimum months from manufacture; minimum remaining shelf life at delivery
Materials: Medical-grade housing; appropriate sterility; filter membrane size/type details
Test/QA: Batch-wise test reports; supplier to provide certifications at bid/supply time
Brand/OEM: OEM authorization required if bidding via distributor
Key Term 1: 25% quantity variation rights during and after contract
Key Term 2: 3 years govt/PSU supply experience required
Key Term 3: ISO 9001 certification and MDR 2017 compliance mandatory
Not explicitly stated; ensure alignment with buyer terms and submission of all required certificates
Delivery period linked to last date of original delivery order; extended time proportional to quantity increase with 30-day minimum
Not specified; ensure bidder clarifies LD clauses for late delivery and non-conformance
3 years of regular manufacture/supply of similar category products to central/state govt or PSU
ISO 9001 certified bidder or OEM
Authorized distributor/OEM authorization where applicable
These are the final prices after the reverse auction event. Prices may be lower than initial bids.
| Rank | Seller | Final Price | Item |
|---|---|---|---|
| L1 | CHANDANA ENTERPRISES(MII) Under PMA Winner | ₹2,77,600 | Item Categories : Transducer Protector (V2) |
| L2 | NEWTECH MEDICAL DEVICES PRIVATE LIMITED (MII) Under PMA | ₹2,78,000 | Item Categories : Transducer Protector (V2) |
| L3 | VAIDIK VENTURES (MII) Under PMA | ₹3,80,000 | Item Categories : Transducer Protector (V2) |
🎉 L1 Winner
CHANDANA ENTERPRISES(MII) Under PMA
Final Price: ₹2,77,600
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Start
01-Sep-2026, 12:00 pm
End
02-Sep-2026, 12:00 pm
Duration: 24 hours
Reverse Auction Document
✅ RA concluded. Check financial results for final rankings.
Quantity
40000
Bid Type
Two Packet Bid
Bid Validity
120 (Days)
Bid Type
Service
Evaluation
Total value wise evaluation
Inspection Required
No
RA Qualification Rule
H1-Highest Priced Bid Elimination
Tech Clarification Time
2 Days
EMD Required
No
MII Purchase Preference
Yes
MII Preference Band
L1+20%
MSE Purchase Preference
No
MSE Exemption/Relaxation
No
Startup Exemption/Relaxation
No
Bid Splitting Applied
No
Min. Avg. Annual Turnover
2
OEM Avg. Turnover
3
Experience Required
3 Year (s)
Arbitration Clause
No
Mediation Clause
No
Tender Category
Goods
Bid To RA
No
Bid To RA Enabled
Yes
Item Category
Transducer Protector (V2) (Q2)
Advisory Bank
State Bank of India
ePBG Percentage
3%
ePBG Duration (Months)
8
Payment Timelines
Payments shall be made to the Seller within 45 days of issue of consignee receipt-cum-acceptance certificate (CRAC) and on-line submission of bills (This is in supersession of 10 days time as provided in clause 12 of GeM GTC)
Max Delivery Days
10000
Delivery Locations
1
Delivery Cities
South Andamans
Delivery Pincodes
744104
| Consignee | Address | City | State | Pincode | Quantity | Delivery Days | Additional Requirement |
|---|---|---|---|---|---|---|---|
| Manoj Das | 744104,Central Medical Store, Directorate of Health Services Andaman & Nicobar Administration | South Andamans | Andaman And Nicobar Islands | 744104 | - | 10000 | - |
End-to-end support — bid preparation, GeM registration, document filing & compliance by industry experts.
Free consultation · 24h response
Main Document
CATALOG Specification
GEM_GENERAL_TERMS_AND_CONDITIONS
GST registration certificate
Permanent Account Number (PAN) card
Audited financial statements for last 3 years or CA certificate on turnover
ISO 9001 certification documents
Medical Device license (for the product) under Drugs and Cosmetic Act 1940
BIS license and type test certificates (if applicable)
OEM authorization or manufacturer authorization forms
Batch test reports per MDR 2017 for supplied products
Advance sample submission plan (if required)
| Category | Specification | Requirement |
|---|---|---|
| GENERAL | Product Description | Transducer Protector |
| GENERAL | Sterility | Sterile and Non-Pyrogenic |
| PRODUCT INFORMATION | Filter Membrane | Hydrophobic Membrane |
| PRODUCT INFORMATION | Size of Filter | 0.2 micron |
| PRODUCT INFORMATION | Media | PTFE |
| PRODUCT INFORMATION | Housing Material (Medical Grade) | ABS |
| PRODUCT INFORMATION | Housing Color | Transparent |
| PRODUCT INFORMATION | Connection | Female Lure Lock / Male Lure Lock |
| PACKAGING | Packing Type | Individual Moisture Proof Packing |
| 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 | Manufacturing unit Certification | 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 |
| CERTIFICATIONS | Submission of all necessary certifications, licenses and test reports to the buyer at the time of bid submission or along with supplies as per buyer requirement | Yes |
| SHELF LIFE | Shelf life from the date of manufacture (months) | 36 Or higher |
| SHELF LIFE | Minimum shelf life of the product at the time of delivery to the consignee | 3/4 th of Total Shelf Life |
| ADVANCE SAMPLE | Agree to provide advance sample of the product for buyer's approval before commencement of supply in case of bidding | Yes |
Key insights about ANDAMAN & NICOBAR tender market
Bidders must meet eligibility criteria including 3 years of govt/PSU supply experience, ISO 9001 certification, MDR 2017 compliance, and provide Medical Device license. Prepare batch test reports and OEM authorizations. Submit advance sample plan, along with BIS/type test certificates, CA turnover proof, and GST/PAN with bid.
Submit Medical Device license under Drugs and Cosmetic Act, MDR batch test reports, ISO 9001 certificates, BIS license, type tests, OEM authorizations, audited financial statements for 3 years, GST and PAN, and experience contracts showing govt/PSU supply.
Delivery aligns with the last date of original order; if quantity increases by up to 25%, extended delivery time is calculated as (Increased quantity / Original quantity) × Original delivery period, with a minimum of 30 days.
Demonstrate 3 years of regular govt/PSU supply of similar products via contracts; provide copies of contracts for each year, and ensure OEM authorization if bidding through distributors; include turnover proof and ISO 9001 status.
Required standards include MDR 2017 compliance, ISO 9001, Medical Device license under Drugs and Cosmetic Act, BIS/type test certificates, and batch test reports for each supplied lot; all must be uploaded with bid or provided at delivery.
Bidder must agree to provide an advance sample for buyer approval before commencing supply; ensure sample matches MDR-compliant specifications and is accompanied by batch test documentation.
Yes. The bidder must demonstrate a minimum average annual turnover over the last three years ending 31st March, supported by audited balance sheets or CA/Cost Accountant certificate; exact turnover threshold is specified in the bid document.
Upload all relevant licenses (Medical Device license, BIS license), ISO 9001, type test certificates, batch MDR test reports, and OEM authorization with bid; prepare to present originals or verifications to the buyer if requested.