PureWick Female External Catheter PWF030

GUDID 20801741143087

PureWick Female External Catheter

C. R. Bard, Inc.

Female wearable urinal, single-use
Primary Device ID20801741143087
NIH Device Record Keyf25be7fb-0af8-4722-bf7a-e57ee3a41d6f
Commercial Distribution StatusIn Commercial Distribution
Brand NamePureWick Female External Catheter
Version Model NumberPWF030
Catalog NumberPWF030
Company DUNS016898496
Company NameC. R. Bard, Inc.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latextrue
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Countertrue

Customer Support Contacts

Phone+1(800)526-4455
Emailmedical.services@crbard.com
Phone+1(800)526-4455
Emailmedical.services@crbard.com
Phone+1(800)526-4455
Emailmedical.services@crbard.com
Phone+1(800)526-4455
Emailmedical.services@crbard.com
Phone+1(800)526-4455
Emailmedical.services@crbard.com
Phone+1(800)526-4455
Emailmedical.services@crbard.com
Phone+1(800)526-4455
Emailmedical.services@crbard.com
Phone+1(800)526-4455
Emailmedical.services@crbard.com
Phone+1(800)526-4455
Emailmedical.services@crbard.com
Phone+1(800)526-4455
Emailmedical.services@crbard.com
Phone+1(800)526-4455
Emailmedical.services@crbard.com
Phone+1(800)526-4455
Emailmedical.services@crbard.com
Phone+1(800)526-4455
Emailmedical.services@crbard.com
Phone+1(800)526-4455
Emailmedical.services@crbard.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100801741143083 [Primary]
GS110801741143080 [Package]
Contains: 00801741143083
Package: CA [30 Units]
In Commercial Distribution
GS120801741143087 [Package]
Contains: 10801741143080
Package: BX [6 Units]
In Commercial Distribution

FDA Product Code

NZUCollector, urine, powered, non indwelling catheter

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-08-14
Device Publish Date2020-08-06

On-Brand Devices [PureWick Female External Catheter]

20801741189054PureWick Female External Catheter, Not Made with Natural Rubber Latex
20801741183618PureWick Female External Catheter, Not Made with Natural Rubber Latex, Kit
10801741163088PureWick Female External Catheter, Not Made with Natural Rubber Latex
20801741143087PureWick Female External Catheter
20801741215937PureWick Female External Catheter

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.