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Employees State Insurance Corporation Nebulizer Mask Procurement Tender MDR 2017 2026

Bid Publish Date

06-Jun-2026, 11:30 am

Bid End Date

16-Jun-2026, 12:00 pm

Value

โ‚น1,10,000

Progress

Issue06-Jun-2026, 11:30 am
AwardPending
Explore all 4 tabs to view complete tender details

Quantity

4000

Bid Type

Two Packet Bid

Categories 3

Tender Overview

The ESIC (Employees State Insurance Corporation) invites bids for the supply of nebulizer masks meeting medical-grade standards. Estimated value is โ‚น110,000. The procurement requires MDR 2017 compliance, a valid medical device license under the Drugs and Cosmetics Act, and manufacturer certification. Bidder must provide an advance sample post-award and two samples for buyer approval within 5 days. An option clause allows a 25% quantity variation at contracted rates, with delivery timelines linked to original orders. This tender emphasizes high-quality, anatomically shaped, flexible masks compatible with all nebulizers, along with proper packaging and shelf-life commitments. Key differentiators include mandatory material test reports and early sample approval procedures. Unique aspects include the need for test reports per MDR 2017 and the delivery schedule adjustment if sample approvals are delayed.

Technical Specifications & Requirements

  • Product type: Nebulizer mask (fexible, anatomically shaped) made from medical-grade material
  • Compatibility: Works with all nebulizer machines; includes standard tube connector and securing mechanism
  • Specifications to confirm: Size, color, medication chamber capacity, air tube length, and number of air tubes
  • Packaging: Defined Type of Packing; advance samples required (2 samples) within 5 days post-award
  • Certifications & testing: MDR 2017 compliance, valid medical device license under Drugs and Cosmetic Act, Manufacturer Certification, batch test reports as per MDR 2017; all certifications/test reports to be submitted at bid and/or with supplies
  • Shelf life: Minimum shelf life at delivery date; minimum shelf life from manufacture date
  • Quality control: Material Test Certificate to accompany delivery; buyer labs to verify acceptance
  • Advance sampling: Samples to be approved before bulk manufacturing; deviations may lead to contract termination or modification

Terms, Conditions & Eligibility

  • Option clause: Delivery/quantity may increase by up to 25% of bid quantity during contract and currency period
  • Scope of supply: Bid price includes all costs for supply of goods; no separate lines for services
  • Sample clause: Two advance samples required; approval or modification list provided within 5 days; delay in approval may extend delivery without LD
  • Documentation: Submit all required certifications, licenses, and test reports with bid and with supplies as required by buyer
  • Material acceptance: Material Test Certificate to be supplied; buyer lab results govern acceptance
  • EMD/Payment: Not specified in data; payment terms not detailed; bidders should verify terms during bidding

Key Specifications

  • Nebulizer mask made of medical-grade material with flexible, anatomically shaped design

  • Must be compatible with all nebulizer machines and include standard tube connector and securing mechanism

  • Provide explicit details for: Size, Color, Medication chamber capacity, Number of Air Tubes, Air Tube Length

  • Packaging type must be defined; include Shelf life from date of manufacture and minimum shelf life on delivery

  • Certifications required: MDR 2017 compliance, valid medical device license under Drugs and Cosmetic Act, Manufacturer Certification, batch test reports per MDR 2017

  • Advance samples: supply 2 samples for approval within 5 days of award; failure to approve could modify delivery schedule

  • Material Test Certificate to accompany delivery; buyer lab evaluates for acceptance, with results final

Terms & Conditions

  • Option clause allows ยฑ25% quantity variation at contracted rates

  • Advance sample requirement: 2 samples within 5 days post-award for buyer approval

  • Mandatory MDR 2017 compliance and medical device licensing with batch test reports

Important Clauses

Payment Terms

Not specified in tender data; verify terms during bidding and align with contract

Delivery Schedule

Delivery starts after approval of advance sample; additional time may be required if sample approval is delayed; option clause may extend delivery timeline

Penalties/Liquidated Damages

LD terms not explicitly stated; ensure clarity on penalties in final contract based on delivery delays

Bidder Eligibility

  • Must hold valid MDR 2017 compliance and medical device license under Drugs and Cosmetic Act

  • Manufacturer Certification and ability to provide batch test reports per MDR 2017

  • Capability to supply with advance sample testing and timely delivery as per terms

Additional Tender Data

Commercial Details

Tender Category

Goods

Bid To RA

No

Bid To RA Enabled

Yes

Item Category

Nebulizer Mask (Q2)

Authority Records

MINISTRY OF LABOUR AND EMPLOYMENT

BID & GeM Expert Consultancy

End-to-end support โ€” bid preparation, GeM registration, document filing & compliance by industry experts.

Bid Preparation GeM Registration Document Filing

Free consultation ยท 24h response

Documents 3

GeM-Bidding-9427644.pdf

Main Document

CATALOG-Specification-1

CATALOG Specification

GEM General Terms and Conditions Document

GEM_GENERAL_TERMS_AND_CONDITIONS

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Technical Specifications 1 Item

Item #1 Details

View Catalog
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 Pediatric
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 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

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Required Documents

1

OEM Authorization Certificate *In case any bidder is seeking exemption from Experience / Turnover Criteria

2

the supporting documents to prove his eligibility for exemption must be uploaded for evaluation by the buyer

Frequently Asked Questions

How to bid for the nebulizer mask tender in ESIC India 2026

Bidders must meet MDR 2017 compliance, possess valid medical device licenses under the Drugs and Cosmetic Act, provide Manufacturer Certification, and submit batch test reports. Include two advance samples within 5 days of award, and comply with the 25% quantity variation option. Ensure all documents accompany the bid.

What documents are required for ESIC nebulizer mask procurement

Required documents include GST registration, PAN card, Medical Device license, MDR 2017 compliance certificates, Manufacturer Certification, batch test reports for each item, material test certificates, and OEM authorization if applicable. Also provide past supply experience and financial statements as requested in terms.

What are the technical specifications for the nebulizer mask

The mask must be medical-grade, flexible and anatomically shaped, compatible with all nebulizers, include standard tube connector and securing mechanism, and specify size, color, medication chamber capacity, and air tube details. Supply must include advance samples for approval.

What are the MDR 2017 certification requirements for this tender

Bidders must provide MDR 2017 compliance evidence, a valid medical device license under the Drugs and Cosmetic Act, and batch test reports per MDR 2017. These certificates should be included with the bid submission and with each supply delivery as required by ESIC.

What is the impact of the 25% option clause in this bid

The purchaser may increase/decrease order quantity by up to 25% of bid quantity at contracted rates during contract and currency. Delivery timelines extend proportionally from the last delivery date, with a minimum extension of 30 days, ensuring orderly supply adjustments.

How to handle advance samples and potential delays in approval

Submit 2 advance samples within 5 days of award. The buyer approves or lists required modifications within 5 days. If approval is delayed, the delivery period is reset without LD for the delay, ensuring fair adjustment while maintaining quality.

What is the expected value and scope of supply for this tender

Estimated value is โ‚น110,000 for the supply of nebulizer masks. The scope is limited to the supply of goods with required packaging, certifications, and batch test reports; services are not included in the bid price.

Where to obtain batch test reports and packaging requirements

Batch test reports must be issued per MDR 2017 and accompany delivery. Packaging type details are specified in the tender; ensure compliance with packaging standards and include Material Test Certificates for each batch.

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