Pomee

FDA UDI

Class I (US FDA UDI)

by Pomee Corporation

Identity

Trade Name: Pomee FDA UDI
Generic Name: ENT soft-tissue cutting forceps FDA UDI
Device Name: Tissue Nippers Goldman Fox 4" 8mm jaw FDA UDI
Model / Reference: 742-2720 FDA UDI
Description: Tissue Nippers Goldman Fox 4" 8mm jaw FDA UDI

Identifiers

Catalog Number: 742-2720 FDA UDI
Primary DI / UDI-DI: G15774227200 FDA UDI
FDA Product Code: HND FDA UDI
GMDN Term: ENT soft-tissue cutting forceps FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 886.4350 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: ENT soft-tissue cutting 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 18889ad6-75e6-43c2-9c3d-6c2cb07e23d4 34 fields · synced May 30, 2026