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Q-Fix

FDA UDI

Class I (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
Q-FIX FDA UDI
Generic Name
Fluted surgical drill bit, single-use FDA UDI
Device Name
1.8MM Q-FIX DISPOSABLE FLEXIBLE DRILL FDA UDI
Model / Reference
72290118 FDA UDI
Description
1.8MM Q-FIX DISPOSABLE FLEXIBLE DRILL FDA UDI

Identifiers

Catalog Number
72290118 FDA UDI
Primary DI / UDI-DI
00885556657447 FDA UDI
FDA Product Code
HTW FDA UDI
GMDN Term
Fluted surgical drill bit, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Fluted surgical drill bit, single-use

Q-Fix by Smith & Nephew, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Fluted surgical drill bit, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI fd5ccf62-ea93-4257-a23c-87679994e005 35 fields · synced Jun 6, 2026