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LINK Instruments - Impactors, extractors and insertion

FDA UDI

Class I (US FDA UDI)

by WALDEMAR LINK GmbH & Co. KG

Identity

Trade Name
LINK Instruments - Impactors, extractors and insertion FDA UDI
Generic Name
Hip prosthesis socket pusher FDA UDI
Device Name
Hip prosthesis socket pusher - Screw-In Acetabular Cup Systems Type K and Type V FDA UDI
Model / Reference
130-839 FDA UDI
Description
Hip prosthesis socket pusher - Screw-In Acetabular Cup Systems Type K and Type V FDA UDI

Identifiers

Primary DI / UDI-DI
04026575034314 FDA UDI
FDA Product Code
HWA FDA UDI
GMDN Term
Hip prosthesis socket pusher FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Hip prosthesis socket pusher

LINK Instruments - Impactors, extractors and insertion by WALDEMAR LINK GmbH & Co. KG — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Hip prosthesis socket pusher.

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 443e2879-746b-4349-b0db-e3cd994810f5 33 fields · synced May 30, 2026