← Back to catalogue

Control

FDA UDI

Class I (US FDA UDI)

by Depuy Orthopaedics, Inc.

Identity

Trade Name
CONTROL FDA UDI
Generic Name
Wire holding/twisting pliers FDA UDI
Device Name
CONTROL CABLE WIRE TENSIONER FDA UDI
Model / Reference
2739-46-000 FDA UDI
Description
CONTROL CABLE WIRE TENSIONER FDA UDI

Identifiers

Catalog Number
273946000 FDA UDI
Primary DI / UDI-DI
10603295152132 FDA UDI
FDA Product Code
HYA FDA UDI
GMDN Term
Wire holding/twisting pliers FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Wire holding/twisting pliers

Control by Depuy Orthopaedics, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wire holding/twisting pliers.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Depuy Orthopaedics, Inc.

Sources (1)

  • FDA UDI f253962d-ac92-4039-9c73-1450a8baad7a 35 fields · synced Jun 8, 2026