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VariAx

FDA UDI

Class II (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
VariAx FDA UDI
Generic Name
Orthopaedic fixation plate, non-bioabsorbable FDA UDI
Device Name
VOLAR SMARTLOCK DR PL.NARROW,RIGHT,LONG FDA UDI
Model / Reference
54-25385S FDA UDI
Description
VOLAR SMARTLOCK DR PL.NARROW,RIGHT,LONG FDA UDI

Identifiers

Catalog Number
54-25385S FDA UDI
Primary DI / UDI-DI
04546540578723 FDA UDI
FDA Product Code
HRS FDA UDI
GMDN Term
Orthopaedic fixation plate, non-bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3030 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Orthopaedic fixation plate, non-bioabsorbable

VariAx by Stryker Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic fixation plate, non-bioabsorbable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stryker Corp.

Sources (1)

  • FDA UDI 81c983b2-bf84-4fe6-8db0-32258e34e017 35 fields · synced Jun 8, 2026