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Avenir® Müller

FDA UDI

Class II (US FDA UDI)

by Zimmer, Inc.

Identity

Trade Name
Avenir® Müller FDA UDI
Generic Name
Coated hip femur prosthesis, modular FDA UDI
Device Name
Avenir Müller stem 1 Lateral FDA UDI
Model / Reference
01.06010.101 FDA UDI
Description
Avenir Müller stem 1 Lateral FDA UDI

Identifiers

Primary DI / UDI-DI
00889024288133 FDA UDI
510(k) Number
K123392 FDA UDI
FDA Product Code
KWZ FDA UDI
KWY FDA UDI
LZO FDA UDI
MEH FDA UDI
LWJ FDA UDI
JDI FDA UDI
GMDN Term
Coated hip femur prosthesis, modular FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3310 FDA UDI
888.3390 FDA UDI
888.3353 FDA UDI
888.3360 FDA UDI
888.3350 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: Coated hip femur prosthesis, modular

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

Similar devices

Also classified as Coated hip femur prosthesis, modular.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Zimmer, Inc.

Sources (1)

  • FDA UDI 964c4804-37ce-46c2-900d-193b6b137850 36 fields · synced May 30, 2026