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Contours VPS Volar Plating System

FDA UDI

Class II (US FDA UDI)

by Orthofix, Inc.

Identity

Trade Name
Contours VPS Volar Plating System FDA UDI
Generic Name
Manual orthopaedic bender, reusable FDA UDI
Device Name
BENDER, STRAIGHT PLATE FDA UDI
Model / Reference
1 FDA UDI
Description
BENDER, STRAIGHT PLATE FDA UDI

Identifiers

Catalog Number
DH0412CE FDA UDI
Primary DI / UDI-DI
18054242516040 FDA UDI
FDA Product Code
HWC FDA UDI
GMDN Term
Manual orthopaedic bender, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3040 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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Manual orthopaedic bender, reusable

Contours VPS Volar Plating System by Orthofix, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Manual orthopaedic bender, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Orthofix, Inc.

Sources (1)

  • FDA UDI 84cf0dc3-8385-4155-8dfd-20168229db3b 35 fields · synced May 30, 2026