Axiom®

FDA UDI

Class I (US FDA UDI)

by Etablissements Anthogyr

Identity

Trade Name: AXIOM® FDA UDI
Generic Name: Screw extractor, reusable FDA UDI
Device Name: UNSCREWING MANDREL Ø0.75 FDA UDI
Model / Reference: INMD075 FDA UDI
Description: UNSCREWING MANDREL Ø0.75 FDA UDI

Identifiers

Primary DI / UDI-DI: 03663394482844 FDA UDI
FDA Product Code: NDP FDA UDI
GMDN Term: Screw extractor, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 872.3980 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

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Screw extractor, reusable

Axiom® by Etablissements Anthogyr — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Medfix — Medfix International, LLC · Class I

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: Etablissements Anthogyr

Sources (1)

FDA UDI 0b57f5c9-5cb3-4a42-af73-64cb583ef224 33 fields · synced May 30, 2026