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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
Gingival retraction cord packing tool FDA UDI
Device Name
Retraction Cord Instrument, Serrated, Double Ended FDA UDI
Model / Reference
Packing 1 SER FDA UDI
Description
Retraction Cord Instrument, Serrated, Double Ended FDA UDI

Identifiers

Primary DI / UDI-DI
00841685104573 FDA UDI
FDA Product Code
DZN FDA UDI
GMDN Term
Gingival retraction cord packing tool 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
Dry Heat Sterilization FDA UDI

Category: Gingival retraction cord packing tool

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

Similar devices

Also classified as Gingival retraction cord packing tool.

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 fa571395-fc0e-4edd-9062-cf0436626373 33 fields · synced Jun 9, 2026