Artman Instruments

FDA UDI

Class I (US FDA UDI)

by Wise Linkers Llc

Identity

Trade Name: Artman Instruments FDA UDI
Generic Name: Dental restoration carver, amalgam, reusable FDA UDI
Device Name: Dental Composite Shaper and Groove Former Carver ARTMAN FDA UDI
Model / Reference: 242390 FDA UDI
Description: Dental Composite Shaper and Groove Former Carver ARTMAN FDA UDI

Identifiers

Catalog Number: 1 FDA UDI
Primary DI / UDI-DI: D1272423901 FDA UDI
FDA Product Code: EIY FDA UDI
GMDN Term: Dental restoration carver, amalgam, reusable 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Dental restoration carver, amalgam, reusable

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

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Wise Linkers Llc

Sources (1)

FDA UDI f6b536b5-1691-4625-8a1c-32b951b8b6e3 34 fields · synced Jun 1, 2026