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MP Reconstruction Prosthesis

FDA UDI

Class II (US FDA UDI)

by WALDEMAR LINK GmbH & Co. KG

Identity

Trade Name
MP Reconstruction Prosthesis FDA UDI
Generic Name
Press-fit hip femur prosthesis, modular FDA UDI
Device Name
Hip Prosthesis Stem,Size S-0 FDA UDI
Model / Reference
172-918/12 FDA UDI
Description
Hip Prosthesis Stem,Size S-0 FDA UDI

Identifiers

Catalog Number
172-918/12 FDA UDI
Primary DI / UDI-DI
04026575320592 FDA UDI
510(k) Number
K142187 FDA UDI
FDA Product Code
LZO FDA UDI
LWJ FDA UDI
JDI 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
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

Category: Press-fit hip femur prosthesis, modular

MP Reconstruction Prosthesis by WALDEMAR LINK GmbH & Co. KG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Cleared under the same submission

K142187 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
WALDEMAR LINK GmbH & Co. KG

Sources (1)

  • FDA UDI 5e6b5f12-1a66-41bd-a887-107b8644c05a 36 fields · synced Jun 8, 2026