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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
Surgical mallet FDA UDI
Device Name
Surgical mallet - General Instrument FDA UDI
Model / Reference
130-686 FDA UDI
Description
Surgical mallet - General Instrument FDA UDI

Identifiers

Primary DI / UDI-DI
04026575033362 FDA UDI
FDA Product Code
FZY FDA UDI
GMDN Term
Surgical mallet 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: Surgical mallet

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 Surgical mallet.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 20e831a8-a2dd-4e59-9f88-0a0640e020ad 33 fields · synced Jun 8, 2026