Novo Surgical

FDA UDI

Class I (US FDA UDI)

by Novo Surgical, Inc.

Identity

Trade Name: Novo Surgical FDA UDI
Generic Name: ENT soft-tissue cutting forceps FDA UDI
Device Name: king adenoid punch forceps, triangular jaw & strongly curved shaft, 6.0 mm upper jaw & 7.0 mm lower basket, 4-1/8" (10.5 cm) shaft FDA UDI
Model / Reference: E8372-80 FDA UDI
Description: king adenoid punch forceps, triangular jaw & strongly curved shaft, 6.0 mm upper jaw & 7.0 mm lower basket, 4-1/8" (10.5 cm) shaft FDA UDI

Identifiers

Catalog Number: E8372-80 FDA UDI
Primary DI / UDI-DI: 00842331195471 FDA UDI
FDA Product Code: KBS FDA UDI
GMDN Term: ENT soft-tissue cutting forceps FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 874.4420 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

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

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: ENT soft-tissue cutting forceps

Novo Surgical by Novo Surgical, 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: Novo Surgical, Inc.

Sources (1)

FDA UDI c93a7075-699d-48fb-bad4-16a149045a6d 35 fields · synced Jun 8, 2026