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OMNI Conical Stem

FDA UDI

Class II (US FDA UDI)

by OMNIlife science, Inc.

Identity

Trade Name
OMNI Conical Stem FDA UDI
Generic Name
Coated hip femur prosthesis, modular FDA UDI
Device Name
Anseris Conical Tapered Stem, Size 3 FDA UDI
Model / Reference
HC-32430 FDA UDI
Description
Anseris Conical Tapered Stem, Size 3 FDA UDI

Identifiers

Catalog Number
HC-32430 FDA UDI
Primary DI / UDI-DI
00841690130192 FDA UDI
FDA Product Code
LZO FDA UDI
LWJ FDA UDI
GMDN Term
Coated hip femur prosthesis, modular FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3353 FDA UDI
888.3360 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Category: Coated hip femur prosthesis, modular

OMNI Conical Stem by OMNIlife science, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Coated hip femur prosthesis, modular.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5a5115de-1055-4ef2-99a3-550d50c70199 35 fields · synced Jun 9, 2026