Identity
- Trade Name
- Lifelong Premium FDA UDI
- Generic Name
- General-purpose syringe/needle FDA UDI
- Device Name
- 01ml Piston Syringe with needle (23Gx1") FDA UDI
- Model / Reference
- C0131 FDA UDI
- Description
- 01ml Piston Syringe with needle (23Gx1") FDA UDI
Identifiers
- Catalog Number
- C0131 FDA UDI
- Primary DI / UDI-DI
- 08906067661944 FDA UDI
- 510(k) Number
- K210103 FDA UDI
- FDA Product Code
- FMF FDA UDIFMI FDA UDI
- GMDN Term
- General-purpose syringe/needle FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5860 FDA UDI880.5570 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
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: General-purpose syringe/needle
Lifelong Premium by Lifelong Meditech Private Limited — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K210103 also covers:
- Lifelong Matrix — LIFELONG MEDITECH PRIVATE LIMITED
- Lifelong Matrix — LIFELONG MEDITECH PRIVATE LIMITED
- Lifelong Matrix — LIFELONG MEDITECH PRIVATE LIMITED
- Lifelong Matrix — LIFELONG MEDITECH PRIVATE LIMITED
- Lifelong Matrix — LIFELONG MEDITECH PRIVATE LIMITED
- Lifelong Matrix — LIFELONG MEDITECH PRIVATE LIMITED
- Lifelong Premium — LIFELONG MEDITECH PRIVATE LIMITED
- McKesson — MCKESSON MEDICAL-SURGICAL INC.
- McKesson — MCKESSON MEDICAL-SURGICAL INC.
- McKesson — MCKESSON MEDICAL-SURGICAL INC.
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Lifelong Meditech Private Limited
Sources (1)
- FDA UDI 05605c5d-0a78-48cf-88c4-e13fe41443df 36 fields · synced May 30, 2026