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Axiom®

FDA UDI

Class II (US FDA UDI)

by Etablissements Anthogyr

Identity

Trade Name
AXIOM® FDA UDI
Generic Name
Surgical instrument/implant rack FDA UDI
Device Name
EMPTY AXIOM ML SURGERY KIT FDA UDI
Model / Reference
INMODOPS3V FDA UDI
Description
EMPTY AXIOM ML SURGERY KIT FDA UDI

Identifiers

Primary DI / UDI-DI
03663394167611 FDA UDI
FDA Product Code
KCT FDA UDI
GMDN Term
Surgical instrument/implant rack FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6850 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical instrument/implant rack

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

Similar devices

Also classified as Surgical instrument/implant rack.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Etablissements Anthogyr

Sources (1)

  • FDA UDI 4b95c820-c9b6-431a-b066-307c2eb6daf0 33 fields · synced May 31, 2026