← Back to catalogue

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
Bone holding forceps FDA UDI
Device Name
Bone holding forceps - Megasystem-C Tumor- and Revision System FDA UDI
Model / Reference
16-0020/01 FDA UDI
Description
Bone holding forceps - Megasystem-C Tumor- and Revision System FDA UDI

Identifiers

Primary DI / UDI-DI
04026575361946 FDA UDI
FDA Product Code
HTD FDA UDI
GMDN Term
Bone holding forceps FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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: Bone holding forceps

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 Bone holding forceps.

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 1955ba2c-3dc4-46e5-9f65-c130b0009b97 33 fields · synced Jun 8, 2026