PureWick Female External Catheter PWF030K

GUDID 20801741183618

PureWick Female External Catheter, Not Made with Natural Rubber Latex, Kit

C. R. Bard, Inc.

Female wearable urinal, single-use Female wearable urinal, single-use Female wearable urinal, single-use Female wearable urinal, single-use Female wearable urinal, single-use Female wearable urinal, single-use Female wearable urinal, single-use Female wearable urinal, single-use Female wearable urinal, single-use Female wearable urinal, single-use Female wearable urinal, single-use Female wearable urinal, single-use Female wearable urinal, single-use Female wearable urinal, single-use
Primary Device ID20801741183618
NIH Device Record Key5ae44c32-a5d5-4dbb-8a95-0fbbbe3a2cf3
Commercial Distribution StatusIn Commercial Distribution
Brand NamePureWick Female External Catheter
Version Model NumberPWF030K
Catalog NumberPWF030K
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 Kittrue
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
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
GS100801741183614 [Primary]
GS110801741183611 [Package]
Contains: 00801741183614
Package: CA [1 Units]
In Commercial Distribution
GS120801741183618 [Package]
Contains: 10801741183611
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

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