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LINK Instruments - Chisel, bone curette, raspatory, rongeur

FDA UDI

Class I (US FDA UDI)

by WALDEMAR LINK GmbH & Co. KG

Identity

Trade Name
LINK Instruments - Chisel, bone curette, raspatory, rongeur FDA UDI
Generic Name
Orthopaedic chisel FDA UDI
Device Name
Orthopaedic prosthesis instrument, reusable - General Instrument FDA UDI
Model / Reference
130-787/05 FDA UDI
Description
Orthopaedic prosthesis instrument, reusable - General Instrument FDA UDI

Identifiers

Primary DI / UDI-DI
04026575234073 FDA UDI
FDA Product Code
FZO FDA UDI
GMDN Term
Orthopaedic chisel 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: Orthopaedic chisel

LINK Instruments - Chisel, bone curette, raspatory, rongeur by WALDEMAR LINK GmbH & Co. KG — Class I — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Orthopaedic chisel.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1332ba14-776a-40f6-ab36-057ebdca1d40 33 fields · synced Jun 8, 2026