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Dental

FDA UDI

Class I (US FDA UDI)

by Timesco Healthcare Limited

Identity

Trade Name
Dental FDA UDI
Generic Name
Tooth extraction forceps FDA UDI
Device Name
Dental Extraction Forceps No: 150A American FDA UDI
Model / Reference
640.325.25 FDA UDI
Description
Dental Extraction Forceps No: 150A American FDA UDI

Identifiers

Catalog Number
640.325.25 FDA UDI
Primary DI / UDI-DI
05055382843368 FDA UDI
FDA Product Code
EMG FDA UDI
GMDN Term
Tooth extraction forceps 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

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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Tooth extraction forceps

Dental by Timesco Healthcare Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tooth extraction forceps.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0f99404b-b1a5-487a-a253-667b3c1c8d42 35 fields · synced Jun 8, 2026