Identity
- Trade Name
- UNOLOK FDA UDI
- Generic Name
- General-purpose syringe/needle FDA UDI
- Device Name
- UNOLOK Single Use Hypodermic Syringe Luer Lock , 3ml with 22G x 1 1/2'' (0.70 X 38mm) Needle, Blister Packed FDA UDI
- Model / Reference
- 3ml (22G x 1 1/2'') FDA UDI
- Description
- UNOLOK Single Use Hypodermic Syringe Luer Lock , 3ml with 22G x 1 1/2'' (0.70 X 38mm) Needle, Blister Packed FDA UDI
Identifiers
- Catalog Number
- 05189 FDA UDI
- Primary DI / UDI-DI
- 08903347051891 FDA UDI
- 510(k) Number
- K945225 FDA UDI
- FDA Product Code
- FMF FDA UDI
- GMDN Term
- General-purpose syringe/needle FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5860 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: General-purpose syringe/needle
Unolok by Hindustan Syringes And Medical Devices Limited — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Hindustan Syringes And Medical Devices Limited
Sources (1)
- FDA UDI 1a0c97be-7ca0-45e9-8de4-1c92cb370e08 35 fields · synced May 30, 2026