← Back to catalogue

Integra®

FDA UDI

Class I (US FDA UDI)

by Integra Lifesciences (ireland) Limited

Identity

Trade Name
Integra® FDA UDI
Generic Name
Electrical-only medical device connection cable, reusable FDA UDI
Device Name
Assembly, Cable S-Video 25 foot, Male/Male Connectors FDA UDI
Model / Reference
600960 FDA UDI
Description
Assembly, Cable S-Video 25 foot, Male/Male Connectors FDA UDI

Identifiers

Catalog Number
600960 FDA UDI
Primary DI / UDI-DI
10381780509189 FDA UDI
FDA Product Code
FWC FDA UDI
GMDN Term
Electrical-only medical device connection cable, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4160 FDA UDI
Commercial Distribution
Not 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Integra® by Integra Lifesciences (ireland) Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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

Sources (1)

  • FDA UDI c6114f18-af69-45fd-90a9-7e2008b51d35 36 fields · synced May 30, 2026