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Axiom®

FDA UDI

Class I (US FDA UDI)

by Etablissements Anthogyr

Identity

Trade Name
AXIOM® FDA UDI
Generic Name
Dental torque wrench FDA UDI
Device Name
SURGICAL DYNAMOMETRIC WRENCH FDA UDI
Model / Reference
INCCDC FDA UDI
Description
SURGICAL DYNAMOMETRIC WRENCH FDA UDI

Identifiers

Primary DI / UDI-DI
03663394011150 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Dental torque wrench 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

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental torque wrench

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

Similar devices

Also classified as Dental torque wrench.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4dbd082b-049f-4d0e-9068-7cb49bdfed6d 33 fields · synced May 31, 2026