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ARGELITE 60 (5 dwt)

FDA UDI

Class II (US FDA UDI)

by Argen Corporation, The

Identity

Trade Name
ARGELITE 60 (5 dwt) FDA UDI
Generic Name
Dental casting noble alloy FDA UDI
Device Name
Alloy other noble metal FDA UDI
Model / Reference
120205 FDA UDI
Description
Alloy other noble metal FDA UDI

Identifiers

Catalog Number
120205 FDA UDI
Primary DI / UDI-DI
D818120205 FDA UDI
FDA Product Code
EJS FDA UDI
GMDN Term
Dental casting noble alloy FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3060 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

No

FDA UDI

Category: Dental casting noble alloy

ARGELITE 60 (5 dwt) by Argen Corporation, The — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental casting noble alloy.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f7abe236-c57a-4d58-9759-cf5a06e654d0 35 fields · synced May 30, 2026