Identity
- Trade Name
- PMI FDA UDI
- Generic Name
- Suture kit, non-medicated FDA UDI
- Device Name
- LACERATION TRAY W/SERRATED FORCEP FDA UDI
- Model / Reference
- K303 FDA UDI
- Description
- LACERATION TRAY W/SERRATED FORCEP FDA UDI
Identifiers
- Catalog Number
- K303 FDA UDI
- Primary DI / UDI-DI
- 00812608021420 FDA UDI
- GMDN Term
- Suture kit, non-medicated FDA UDI
Classification
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
Yes
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
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
Yes
FDA UDI
Category: Suture kit, non-medicated
Pmi by Progressive Medical, Inc. — 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 | N/A | Pending data |
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Manufacturer
- Manufacturer
- Progressive Medical, Inc.
Sources (1)
- FDA UDI c2ff99e1-9c67-43a4-85a6-8083e19a9058 35 fields · synced Jun 1, 2026