Tools

FDA UDI

Class II (US FDA UDI)

by A.b. Dental Devices Ltd

Identity

Trade Name: Tools FDA UDI
Generic Name: Surgical screwdriver, reusable FDA UDI
Device Name: Ratchet Hex Driver for I6B FDA UDI
Model / Reference: T3-I6B-S FDA UDI
Description: Ratchet Hex Driver for I6B FDA UDI

Identifiers

Catalog Number: T3-I6B-S FDA UDI
Primary DI / UDI-DI: 07290111274428 FDA UDI
FDA Product Code: NHA FDA UDI
GMDN Term: Surgical screwdriver, reusable FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 872.3630 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

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: Surgical screwdriver, reusable

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

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: A.b. Dental Devices Ltd

Sources (1)

FDA UDI fec59699-5bfd-4982-b708-73dcc1436512 35 fields · synced May 30, 2026