← Back to catalogue

Avenir®

FDA UDI

Class II (US FDA UDI)

by Zimmer, Inc.

Identity

Trade Name
Avenir® FDA UDI
Generic Name
Uncoated hip femur prosthesis, modular FDA UDI
Device Name
Avenir® Standard stem cemented 1 FDA UDI
Model / Reference
01.06010.201 FDA UDI
Description
Avenir® Standard stem cemented 1 FDA UDI

Identifiers

Primary DI / UDI-DI
00889024288225 FDA UDI
510(k) Number
K131884 FDA UDI
FDA Product Code
KWZ FDA UDI
KWY FDA UDI
KWL FDA UDI
LZO FDA UDI
GMDN Term
Uncoated hip femur prosthesis, modular FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3310 FDA UDI
888.3390 FDA UDI
888.3360 FDA UDI
888.3353 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

Yes

FDA UDI

Category: Uncoated hip femur prosthesis, modular

Avenir® by Zimmer, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Uncoated hip femur prosthesis, modular.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Zimmer, Inc.

Sources (1)

  • FDA UDI 4c33bbd6-ca72-424f-8a40-4f4d450436bd 36 fields · synced Jun 1, 2026