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Virage Navigation System

FDA UDI

Class II (US FDA UDI)

by Zimmer Biomet

Identity

Trade Name
Virage Navigation System FDA UDI
Generic Name
General internal orthopaedic fixation system implantation kit FDA UDI
Device Name
Drill Guide Reference Array FDA UDI
Model / Reference
131T3001 FDA UDI
Description
Drill Guide Reference Array FDA UDI

Identifiers

Primary DI / UDI-DI
03662663063494 FDA UDI
510(k) Number
K240647 FDA UDI
FDA Product Code
OLO FDA UDI
GMDN Term
General internal orthopaedic fixation system implantation kit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4560 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: General internal orthopaedic fixation system implantation kit

Virage Navigation System by Zimmer Biomet — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General internal orthopaedic fixation system implantation kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Zimmer Biomet

Sources (1)

  • FDA UDI 276b62a9-f1a6-43aa-8e63-d94920eaf079 34 fields · synced Jun 1, 2026