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Incontinence Clamp

FDA UDI

Class I (US FDA UDI)

by C. R. Bard, Inc.

Identity

Trade Name
Incontinence Clamp FDA UDI
Generic Name
Incontinence penis clamp, reusable FDA UDI
Device Name
Cunningham Incontinence Clamp, Large FDA UDI
Model / Reference
004054 FDA UDI
Description
Cunningham Incontinence Clamp, Large FDA UDI

Identifiers

Catalog Number
004054 FDA UDI
Primary DI / UDI-DI
00801741072765 FDA UDI
FDA Product Code
FHA FDA UDI
GMDN Term
Incontinence penis clamp, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.5160 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

Yes

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

No

FDA UDI

Category: Incontinence penis clamp, reusable

Incontinence Clamp by C. R. Bard, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Incontinence penis clamp, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
C. R. Bard, Inc.

Sources (1)

  • FDA UDI 8f151c75-c5e1-47db-87e2-b90faf060bfa 35 fields · synced May 31, 2026