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Pomee

FDA UDI

Class I (US FDA UDI)

by Pomee Corporation

Identity

Trade Name
Pomee FDA UDI
Generic Name
Dental dressing forceps, reusable FDA UDI
Device Name
RING FORCEPS FDA UDI
Model / Reference
PCRF FDA UDI
Description
RING FORCEPS FDA UDI

Identifiers

Catalog Number
PCRF FDA UDI
Primary DI / UDI-DI
G157PCRF0 FDA UDI
FDA Product Code
EIE FDA UDI
GMDN Term
Dental dressing forceps, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6300 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 dressing forceps, reusable

Pomee by Pomee Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental dressing forceps, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Pomee Corporation

Sources (1)

  • FDA UDI 4116d1b6-4e0e-43f7-9361-62a5a5e89c0d 34 fields · synced Jun 1, 2026