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Artman Instruments

FDA UDI

Class I (US FDA UDI)

by Wise Linkers Llc

Identity

Trade Name
Artman Instruments FDA UDI
Generic Name
Spring-loaded dental mallet FDA UDI
Device Name
Dental Automatic Crown Remover Titanium Spring Loaded Gun Set of 6 ARTMAN FDA UDI
Model / Reference
242304 FDA UDI
Description
Dental Automatic Crown Remover Titanium Spring Loaded Gun Set of 6 ARTMAN FDA UDI

Identifiers

Catalog Number
1 FDA UDI
Primary DI / UDI-DI
D1272423041 FDA UDI
FDA Product Code
EIS FDA UDI
GMDN Term
Spring-loaded dental mallet FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 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

No

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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Spring-loaded dental mallet

Artman Instruments by Wise Linkers Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Spring-loaded dental mallet.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Wise Linkers Llc

Sources (1)

  • FDA UDI 3389f23e-f00f-4e8c-a28d-ef4d4132da09 34 fields · synced May 31, 2026