Nebulizer Mask,Nebulizer Mask
Employees State Insurance Corporation (esic)
VARANASI, UTTAR PRADESH
Bid Publish Date
09-Feb-2026, 7:51 pm
Bid End Date
19-Feb-2026, 8:00 pm
Location
Progress
Quantity
2700
Category
Nebulizer Mask
Bid Type
Two Packet Bid
The Health Department Andaman & Nicobar invites bids for nebulizer masks intended for general medical use within the South Andaman region (postal code 744101). The procurement emphasizes MDR 2017 compliance, medical device licensing, and batch test reports. Bidders must demonstrate OEM authorization, provide advance samples post-award, and ensure shelf life meets delivery requirements. The scope includes masks with medical-grade material, flexible anatomically shaped design, and compatibility with all nebulizer machines. The call emphasizes supplier capability to meet regulatory certifications and timely delivery. The opportunity is defined by mandatory certifications, manufacturer validation, and batch-wise testing, with critical supply chain controls and quality documentation. The contract requires clear demonstration of prior government supply experience and adherence to seller liability terms, including non-assignment and sub-contract restrictions.
Product: Nebulizer mask
Material: medical grade; sterile; flexible anatomically shaped
Compatibility: works with all nebulizer machines
Standards: MDR 2017 compliance; Drugs and Cosmetic Act licensing
Packaging: specified packing type; advance sample provision
Shelf life: minimum shelf life at delivery; date of manufacture
Chambers: medication chamber count and capacity; air tube length; standard tube connector
Securing mechanism: secure fit to user face
EMD as per GeM terms; PBG or fixed deposit allowed
3 years government supply experience with contract proofs
Authorized OEM distribution with certificate and details
Delivery within stipulated period; termination rights for non-compliance
Advance samples post-award; MDR 2017 and MD licensing required
Payment terms aligned with buyer approvals; security deposit or PBG required; FDR option allowed per GeM norms
Delivery deadlines to be specified; penalties/LD apply for late or incomplete deliveries
Contract may be terminated for non-compliance; LDs may apply for delays or defective materials
Minimum 3 years experience in supplying similar medical devices to government bodies
OEM authorization or manufacturer/supplier with government contracts
Compliance with MDR 2017 and Drugs and Cosmetics Act licensing
Main Document
CATALOG Specification
CATALOG Specification
GEM_GENERAL_TERMS_AND_CONDITIONS
Employees State Insurance Corporation (esic)
VARANASI, UTTAR PRADESH
Employees State Insurance Corporation (esic)
BANGALORE, KARNATAKA
North Eastern Railway
LUCKNOW, UTTAR PRADESH
Employees State Insurance Corporation
Employees State Insurance Corporation
Tender Results
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| Category | Specification | Requirement |
|---|---|---|
| GENERAL | Product Name | Nebulizer Mask |
| GENERAL | Usage | Disposable (Single-Use) |
| GENERAL | Sterility | Sterile |
| TECHNICAL INFORMATION | Material (Medical Grade) | Polyvinyl Chloride (PVC) |
| TECHNICAL INFORMATION | Fexible, anatomical shaped mask | Yes |
| TECHNICAL INFORMATION | Size | Adult |
| TECHNICAL INFORMATION | Compatible with all types of nebulizer machines | Yes |
| TECHNICAL INFORMATION | Color | Transparent |
| TECHNICAL INFORMATION | Number of Medication Chamber | 1 |
| TECHNICAL INFORMATION | Medication chamber capacity | 5 mL to 10 mL |
| TECHNICAL INFORMATION | Number of Air Tube | 1 |
| TECHNICAL INFORMATION | Air Tube Length | 150 cm to 200 cm |
| TECHNICAL INFORMATION | Standard tube connector | Yes |
| TECHNICAL INFORMATION | Securing Mechanism of the mask | Elastic Strap |
| PACKAGING | Type fo Packing | 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 | Manufacturer Certification | ISO:13485 (Latest) |
| CERTIFICATIONS | Availability of Test Report for each supplied batch/product as per Medical Device Rules (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 and/or along with supplies as per buyer requirement | Yes |
| SHELF LIFE | Shelf life from the date of manufacture | 36, 60 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 after award of contract and before commencement of supply in case of bidding only | Yes |
Discover companies most likely to bid on this tender
GST certificate
PAN card
OEM authorization certificate
Manufacturer certification
Experience certificates for government/PSU supply (3 years)
Contract copies of similar supplies
Test reports as per MDR 2017
Bid submission certifications/licenses as per buyer requirement
EMD document or equivalent security deposit
Technical compliance certificates
Key insights about ANDAMAN & NICOBAR tender market
Bidders must meet 3+ years of government medical device supply experience, provide OEM authorization, and submit MDR 2017 compliance certificates along with advance sample post-award. Include EMD, GST, PAN, and batch test reports; ensure delivery within the specified period and comply with non-assignment terms.
Submit GST registration, PAN, manufacturer authorization, MDR compliance certificates, medical device license under Drugs and Cosmetics Act, 3 years government contracts, batch test reports, and bid-form technical and commercial documents; provide contract copies as proof of prior supply.
Devices must use medical-grade material, be sterilized, feature flexible anatomical masks, be compatible with all nebulizers, include appropriate medication chambers and air tubes, standard tube connectors, and secure attachment mechanisms; include MDR 2017 compliance certificates and batch test reports.
Delivery timelines are defined in the buyer terms; ensure adherence to stipulated delivery period; late delivery may incur liquidated damages and potential contract termination per terms.
EMD details follow GeM guidelines; payment terms may include security deposit or PBG; FDR option is allowed; payment is aligned with supply acceptance and contract milestones after successful delivery and certification checks.
Distributors must provide OEM authorization with contact details, manufacturer's certification, and ensure product MDR 2017 compliance; include license validity and test reports for each batch supplied.
Bidders must ensure minimum shelf life at delivery as per MDR guidelines; provide manufacture date, expiry date, and batch-level shelf-life certification to prevent expired stock from being accepted.
Agree to furnish an advance sample post-award; submit the sample for buyer evaluation before commencing supply; ensure the sample aligns with MDR standards and confirms compatibility with nebulizer devices.
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Main Document
CATALOG Specification
CATALOG Specification
GEM_GENERAL_TERMS_AND_CONDITIONS