MSI Precision Specialty Instruments

FDA UDI

Class I (US FDA UDI)

by Med Saver, Inc.

Identity

Trade Name: MSI Precision Specialty Instruments FDA UDI
Generic Name: ENT soft-tissue cutting forceps FDA UDI
Device Name: Antrum Punch, Adult, Backward Through-Cutting, Right Side Cutting, 2.5mm x 4mm Bite, Luer Lock, Working Length 4" (100mm) FDA UDI
Model / Reference: 232-I00-14-LL FDA UDI
Description: Antrum Punch, Adult, Backward Through-Cutting, Right Side Cutting, 2.5mm x 4mm Bite, Luer Lock, Working Length 4" (100mm) FDA UDI

Identifiers

Primary DI / UDI-DI: 00194613029364 FDA UDI
FDA Product Code: KAW 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

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Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: ENT soft-tissue cutting forceps

MSI Precision Specialty Instruments by Med Saver, 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: Med Saver, Inc.

Sources (1)

FDA UDI 5daba10e-9d00-4fb0-a05f-2f86ae43b646 34 fields · synced Jun 8, 2026