Disposable Drill Kit

FDA UDI

Class II (US FDA UDI)

by Ad-Tech Medical Instrument Corp.

Identity

Trade Name: Disposable Drill Kit FDA UDI
Generic Name: Fluted surgical drill bit, single-use FDA UDI
Model / Reference: DDK2-2.4-16X FDA UDI

Identifiers

Catalog Number: DDK2-2.4-16X FDA UDI
Primary DI / UDI-DI: 00841823101143 FDA UDI
FDA Product Code: HBG FDA UDI
HBE FDA UDI
GMDN Term: Fluted surgical drill bit, single-use FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 882.4300 FDA UDI
882.4310 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

MRI Safety

MR Unsafe FDA UDI

Category: Fluted surgical drill bit, single-use

Disposable Drill Kit by Ad-Tech Medical Instrument Corp. — 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: Ad-Tech Medical Instrument Corp.

Sources (1)

FDA UDI 99bf1525-f5ad-4210-83ce-80f5e7544a3e 35 fields · synced Jun 9, 2026