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CUSA Clarity®

FDA UDI

Class U (US FDA UDI)

by Integra Lifesciences (ireland) Limited

Identity

Trade Name
CUSA Clarity® FDA UDI
Generic Name
Electromechanical device/system transport trolley FDA UDI
Device Name
CUSA Clarity® Cart FDA UDI
Model / Reference
C7007P FDA UDI
Description
CUSA Clarity® Cart FDA UDI

Identifiers

Primary DI / UDI-DI
10381780357438 FDA UDI
FDA Product Code
LFL FDA UDI
LBK FDA UDI
GMDN Term
Electromechanical device/system transport trolley FDA UDI

Classification

Device Class
U 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Electromechanical device/system transport trolley

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

Similar devices

Also classified as Electromechanical device/system transport trolley.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Integra Lifesciences (ireland) Limited

Sources (1)

  • FDA UDI df5bacb6-4f26-4020-b074-63060e4a57a8 34 fields · synced Jun 6, 2026