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Variax

FDA UDI

Class I (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
VARIAX FDA UDI
Generic Name
Fluted surgical drill bit, single-use FDA UDI
Device Name
Drill Bit, AO, Scaled FDA UDI
Model / Reference
703691S FDA UDI
Description
Drill Bit, AO, Scaled FDA UDI

Identifiers

Catalog Number
703691S FDA UDI
Primary DI / UDI-DI
07613327071771 FDA UDI
FDA Product Code
LXH 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

Dimensions & Sizes

Size
Length — 122.0 Millimeter FDA UDI

Category: Fluted surgical drill bit, single-use

Variax by Stryker Corp. — 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

Manufacturer
Stryker Corp.

Sources (1)

  • FDA UDI c2f11cbf-3ee9-4a08-bbdc-01638681cc64 35 fields · synced Jun 7, 2026