PureWick Male PWM030

GUDID 10801741219150

PureWick Male External Catheter Kit

C. R. Bard, Inc.

Urinary incontinence penis sheath/port, single-use
Primary Device ID10801741219150
NIH Device Record Keyb861bef3-46f3-4944-9b55-7d9999ebff8f
Commercial Distribution StatusIn Commercial Distribution
Brand NamePureWick Male
Version Model NumberPWM030
Catalog NumberPWM030
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

Device Identifiers

Device Issuing AgencyDevice ID
GS100801741219153 [Primary]
GS110801741219150 [Package]
Contains: 00801741219153
Package: CA [30 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 Date2022-08-09
Device Publish Date2022-08-01

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