Chhattisgarh Health & Family Welfare Department Sterile Hypodermic Syringes Tender 2025 IS 10258 Part 1
N/a
Raigarh, CHHATTISGARH
Bid Publish Date
29-Jun-2026, 9:00 am
Bid End Date
09-Jul-2026, 9:00 am
Location
Progress
Quantity
31500
Category
Single Use Sterile Hypodermic Syringes for Human Use Conforming to IS 10258 (Part 1)
Bid Type
Two Packet Bid
Needle included with syringe
Needle cap or shield to protect the needle
Nominal capacity of syringe specified (ml)
Number of pieces per pack
Residual shelf life at delivery
Color coding per IS/ISO 10555-5
Packing and marking per IS 4605 (latest revision)
Compliance with Drugs and Cosmetic Act 1940 and MDR 2017
Valid Medical Device license/registration number
EMD amount or percentage required; payment terms to be specified
Delivery quantity may vary up to 25% with extended schedule
Mandatory MDR 2017 and Drugs and Cosmetic Act compliance
EMD and payment terms as per standard PMT; extended delivery possible with option clause invoked
Delivery starts after original order; additional time calculated as (increased quantity/original quantity) × original delivery period with minimum 30 days
Penalties for late delivery as per contract terms; LD rates unspecified in data
Proven ability to supply IS 10258/IS 4605/IS ISO 10555 compliant devices
Valid medical device license/registration per Drugs and Cosmetic Act
MDR 2017 compliance and appropriate labeling/packaging
Experience certificates for similar procurement
Tender Category
Goods
Bid To RA
No
Bid To RA Enabled
Yes
Item Category
Single Use Sterile Hypodermic Syringes for Human Use Conforming to IS 10258 (Part 1) (Q2) , Crepe Bandage Conforming to IS 4605 (Q2) , Over-Needle Peripheral Catheters (Intravascular Catheters - Sterile and Single Use) Conforming to IS/ISO 10555 (Part 5) (Q2)
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Main Document
CATALOG Specification
CATALOG Specification
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CATALOG Specification
CATALOG Specification
CATALOG Specification
CATALOG Specification
CATALOG Specification
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CATALOG Specification
OTHER
OTHER
ATC
GEM_GENERAL_TERMS_AND_CONDITIONS
N/a
Raigarh, CHHATTISGARH
N/a
BHOPAL, MADHYA PRADESH
N/a
LUCKNOW, UTTAR PRADESH
Employees State Insurance Corporation (esic)
JAIPUR, RAJASTHAN
Kandla Port Trust
KACHCHH, GUJARAT
Tender Results
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| Category | Specification | Requirement |
|---|---|---|
| PRODUCT INFORMATION | Needle included | Yes |
| PRODUCT INFORMATION | Needle cap or shield to protect the needle | Yes |
| PRODUCT INFORMATION | Nominal Capacity of Syringe (ml) | < 2 |
| PACKAGING | Number of pieces in a Pack | 100 |
| SHELF LIFE | Residual shelf life of the product | Agree to provide residual shelf life of atleast 75% of total shelf life at the time of delivery to the consignee |
| CERTIFICATIONS | Compliance to Drugs and Cosmetic Act 1940 and 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 | Yes |
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GST registration certificate
PAN card
Experience certificates for supplying similar medical devices
Financial statements or turnover evidence
EMD payment proof
Technical bid submission documents
OEM authorization letter (if applicable)
Medical device license/registration number
MDR compliance certificates
Packaging and marking compliance documentation (IS 4605)
Bidders must submit GST, PAN, experience certificates and MDR/compliance documents, along with EMD proof and OEM authorizations. Ensure IS/ISO standards compliance, IS 4605 packaging, and valid medical device license. Follow option clause terms for quantity adjustments up to 25%.
Required documents include GST certificate, PAN, experience certificates for similar devices, financial statements, EMD proof, technical bid, OEM authorization, medical device license/registration, MDR compliance, and IS 4605 packaging documentation.
Products must conform to IS 10258 (Part 1) for syringes, IS/ISO 10555 (Part 5) for catheters, IS 4605 for packaging, and MDR 2017 with Drugs and Cosmetic Act compliance; color coding follows IS/ISO 10555-5.
Packaging must adhere to IS 4605 latest revision, with precise packing and marking; ensure packaging integrity and traceability for each pack containing syringe and catheter components.
The buyer may increase or decrease quantity by up to 25% of bid quantity at contract placement and during currency, with extended delivery time calculated as (additional quantity/original quantity) × original delivery period, minimum 30 days.
A valid Medical Device license/registration number issued by the competent authority is required; ensure MDR 2017 compliance and Drugs and Cosmetic Act adherence for all listed products.
Verify color coding per IS/ISO 10555-5 Table 1, and confirm catheter features: wings, injection port, lumen count, and nominal outside diameter; ensure these match the tender’s product information.
Exact bid submission deadlines are not provided in the data; bidders should monitor official tender portals for updates and ensure MDR-compliant documentation is prepared in advance.
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Main Document
CATALOG Specification
CATALOG Specification
CATALOG Specification
CATALOG Specification
CATALOG Specification
CATALOG Specification
CATALOG Specification
CATALOG Specification
CATALOG Specification
CATALOG Specification
CATALOG Specification
OTHER
OTHER
ATC
GEM_GENERAL_TERMS_AND_CONDITIONS