FDA UDI In Commercial Distribution 🇺🇸 United States

PureWick

DI: 00801741226960 · Model: PWF030FX · C. R. Bard, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

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Basic Information

Brand Name
PureWick
Primary DI
00801741226960
Version / Model
PWF030FX
Catalog Number
PWF030FX
Company Name
C. R. Bard, Inc.
Labeler DUNS
016898496
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-07-29
Public Version
1
Public Version Date
2024-08-06
Public Version Status
New
Public Device Record Key
b97f307c-6a32-4c8e-ba29-40f17ac766bf

Device Description

PureWick Flex Female External Catheter, Acute Care

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
MRI Safety
MR Conditional
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
NZU Collector, urine, powered, non indwelling catheter

GMDN Terms

Code Name
61157 Female wearable urinal, single-use

Identifiers

Type ID
Package 10801741226967
Primary 00801741226960
Package 20801741226964

Customer Contacts