Identity
- Trade Name
- Pomee FDA UDI
- Generic Name
- Dental articulation paper forceps FDA UDI
- Device Name
- Articulting Paper Forceps 6" Curved & Serrated FDA UDI
- Model / Reference
- 708-310 FDA UDI
- Description
- Articulting Paper Forceps 6" Curved & Serrated FDA UDI
Identifiers
- Catalog Number
- 708-310 FDA UDI
- Primary DI / UDI-DI
- G1577083100 FDA UDI
- FDA Product Code
- EFK FDA UDI
- GMDN Term
- Dental articulation paper forceps FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.4565 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
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: Dental articulation paper forceps
Pomee by Pomee Corporation — 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
- Pomee Corporation
Sources (1)
- FDA UDI dbaf3755-42fc-4bf1-8301-11676d8e907c 34 fields · synced May 30, 2026