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Alloclassic® Zweymüller®

FDA UDI

Class II (US FDA UDI)

by Zimmer, Inc.

Identity

Trade Name
Alloclassic® Zweymüller® FDA UDI
Generic Name
Press-fit hip femur prosthesis, modular FDA UDI
Model / Reference
01.00121.040 FDA UDI

Identifiers

Catalog Number
01.00121.040 FDA UDI
Primary DI / UDI-DI
00889024590335 FDA UDI
FDA Product Code
LZO FDA UDI
KWL FDA UDI
JDI FDA UDI
KWY FDA UDI
GMDN Term
Press-fit hip femur prosthesis, modular FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3353 FDA UDI
888.3360 FDA UDI
888.3350 FDA UDI
888.3390 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
MRI Safety
MR Conditional FDA UDI

Category: Press-fit hip femur prosthesis, modular

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

Similar devices

Also classified as Press-fit hip femur prosthesis, modular.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Zimmer, Inc.

Sources (1)

  • FDA UDI 4b12272a-3ad8-425b-b8ed-261c9a84b145 35 fields · synced May 30, 2026