← Back to catalogue

MobileLink Acetabular Cup System - Instruments

FDA UDI

Class II (US FDA UDI)

by WALDEMAR LINK GmbH & Co. KG

Identity

Trade Name
MobileLink Acetabular Cup System - Instruments FDA UDI
Generic Name
Surgical implant handling forceps FDA UDI
Device Name
Surgical implant handling forceps - MobileLink Acetabular Cup System FDA UDI
Model / Reference
183-950/01 FDA UDI
Description
Surgical implant handling forceps - MobileLink Acetabular Cup System FDA UDI

Identifiers

Primary DI / UDI-DI
04026575274222 FDA UDI
510(k) Number
K200607 FDA UDI
FDA Product Code
OQG FDA UDI
LPH FDA UDI
GMDN Term
Surgical implant handling forceps FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3358 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

No

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: Surgical implant handling forceps

MobileLink Acetabular Cup System - Instruments by WALDEMAR LINK GmbH & Co. KG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical implant handling forceps.

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

Sources (1)

  • FDA UDI 3878ccb5-dd63-4ed9-b9d6-49aafb50ce18 34 fields · synced Jun 8, 2026