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A. Titan Instruments

FDA UDI

Class I (US FDA UDI)

by A.Titan Instruments

Identity

Trade Name
A. Titan Instruments FDA UDI
Generic Name
Dental amalgam carrier FDA UDI
Device Name
Amalgam carrier, double ended, carbide FDA UDI
Model / Reference
Standard C FDA UDI
Description
Amalgam carrier, double ended, carbide FDA UDI

Identifiers

Primary DI / UDI-DI
00841685103545 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Dental amalgam carrier FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3980 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
Dry Heat Sterilization FDA UDI

Category: Dental amalgam carrier

A. Titan Instruments by A.Titan Instruments — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental amalgam carrier.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
A.Titan Instruments

Sources (1)

  • FDA UDI f87c901d-9977-46b3-8736-d741b0f650aa 33 fields · synced Jun 9, 2026