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Dvr® Crosslockdistal Volar Radius Plate Medium Right

FDA UDI

Class II (US FDA UDI)

by Biomet Orthopedics, Inc.

Identity

Trade Name
DVR® CROSSLOCKDISTAL VOLAR RADIUS PLATE MEDIUM RIGHT FDA UDI
Generic Name
Orthopaedic fixation plate kit, non-bioabsorbable, non-antimicrobial FDA UDI
Model / Reference
811812060 FDA UDI

Identifiers

Catalog Number
811812060 FDA UDI
Primary DI / UDI-DI
00887868105456 FDA UDI
FDA Product Code
LXT FDA UDI
GMDN Term
Orthopaedic fixation plate kit, non-bioabsorbable, non-antimicrobial 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Orthopaedic fixation plate kit, non-bioabsorbable, non-antimicrobial

Dvr® Crosslockdistal Volar Radius Plate Medium Right by Biomet Orthopedics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic fixation plate kit, non-bioabsorbable, non-antimicrobial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Biomet Orthopedics, Inc.

Sources (1)

  • FDA UDI a6c8ced0-efc6-4529-9d1a-4a46aac4b09a 35 fields · synced May 30, 2026