← Back to catalogue

Extension Tubing

FDA UDI

Class I (US FDA UDI)

by C. R. Bard, Inc.

Identity

Trade Name
Extension Tubing FDA UDI
Generic Name
Penis wearable urinal FDA UDI
Device Name
Extension Tubing, For use with Male External Catheters FDA UDI
Model / Reference
650615 FDA UDI
Description
Extension Tubing, For use with Male External Catheters FDA UDI

Identifiers

Catalog Number
650615 FDA UDI
Primary DI / UDI-DI
00801741050978 FDA UDI
FDA Product Code
NNW FDA UDI
GMDN Term
Penis wearable urinal FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.5250 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Penis wearable urinal

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

Similar devices

Also classified as Penis wearable urinal.

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
C. R. Bard, Inc.

Sources (1)

  • FDA UDI 3c28c6fc-05f9-4eee-af2c-d84817b4256a 35 fields · synced May 30, 2026