PureWick Female External Catheter PWFX30

GUDID 20801741189054

Female wearable urinal, single-use

Primary Device ID	20801741189054
NIH Device Record Key	ea35649e-cf2e-46c8-b950-30a91a7549c9
Commercial Distribution Status	In Commercial Distribution
Brand Name	PureWick Female External Catheter
Version Model Number	PWFX30
Catalog Number	PWFX30
Company DUNS	016898496
Company Name	C. R. Bard, Inc.
Device Count	1
DM Exempt	false
Pre-market Exempt	true
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	true
Lot Batch	true
Serial Number	false
Manufacturing Date	false
Expiration Date	true
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	true
RX Perscription	false
OTC Over-The-Counter	true

Device Issuing Agency	Device ID
GS1	00801741189050 [Primary]
GS1	10801741189057 [Package] Contains: 00801741189050 Package: CA [1 Units] In Commercial Distribution
GS1	20801741189054 [Package] Contains: 10801741189057 Package: BX [6 Units] In Commercial Distribution

NZU	Collector, urine, powered, non indwelling catheter

Steralize Prior To Use	false
Device Is Sterile	false

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10801741163088	PureWick Female External Catheter, Not Made with Natural Rubber Latex
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