Identity
- Trade Name
- Mabis FDA UDI
- Generic Name
- Dressing/utility forceps, tweezers-like, reusable FDA UDI
- Device Name
- KELLY FORCEPS CURVED FDA UDI
- Model / Reference
- 25-275-000 FDA UDI
- Description
- KELLY FORCEPS CURVED FDA UDI
Identifiers
- Catalog Number
- 25-725-000 FDA UDI
- Primary DI / UDI-DI
- 00767056257252 FDA UDI
- FDA Product Code
- GEN FDA UDI
- GMDN Term
- Dressing/utility forceps, tweezers-like, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
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
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Dressing/utility forceps, tweezers-like, reusable
Mabis by Dms Holdings, Inc., — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- Dms Holdings, Inc.,
Sources (1)
- FDA UDI 9f4d4621-33f8-4ad2-8bf2-740b91de2fe0 34 fields · synced Jun 1, 2026