Gyrus ACMI

FDA UDI

Class I (US FDA UDI)

by Gyrus Acmi, Inc.

Identity

Trade Name: Gyrus ACMI FDA UDI
Generic Name: ENT soft-tissue cutting forceps FDA UDI
Device Name: 20 DEGREE BLADE ANGLE 2.18 MM BLADE LENGTH FDA UDI
Model / Reference: 130045 FDA UDI
Description: 20 DEGREE BLADE ANGLE 2.18 MM BLADE LENGTH FDA UDI

Identifiers

Primary DI / UDI-DI: 00821925011595 FDA UDI
FDA Product Code: LRC 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

Yes

FDA UDI

Category: ENT soft-tissue cutting forceps

Gyrus ACMI by Gyrus Acmi, 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: Gyrus Acmi, Inc.

Sources (1)

FDA UDI f7ad5f41-189d-438c-ae9b-c4d94c44be00 33 fields · synced May 29, 2026