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Tools

FDA UDI

Class I (US FDA UDI)

by A.b. Dental Devices Ltd

Identity

Trade Name
Tools FDA UDI
Generic Name
Dental implantation depth/angle gauge, reusable FDA UDI
Device Name
Depth Gauge FDA UDI
Model / Reference
T9 FDA UDI
Description
Depth Gauge FDA UDI

Identifiers

Catalog Number
T9 FDA UDI
Primary DI / UDI-DI
07290107274883 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Dental implantation depth/angle gauge, reusable 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental implantation depth/angle gauge, reusable

Tools by A.b. Dental Devices Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental implantation depth/angle gauge, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
A.b. Dental Devices Ltd

Sources (1)

  • FDA UDI 846b9837-3a66-4b59-85a2-82730031d230 35 fields · synced Jun 1, 2026