Primary Device ID | 10801741219150 |
NIH Device Record Key | b861bef3-46f3-4944-9b55-7d9999ebff8f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PureWick Male |
Version Model Number | PWM030 |
Catalog Number | PWM030 |
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 | true |
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 |
Phone | +1(800)526-4455 |
medical.services@crbard.com | |
Phone | +1(800)526-4455 |
medical.services@crbard.com | |
Phone | +1(800)526-4455 |
medical.services@crbard.com | |
Phone | +1(800)526-4455 |
medical.services@crbard.com | |
Phone | +1(800)526-4455 |
medical.services@crbard.com | |
Phone | +1(800)526-4455 |
medical.services@crbard.com | |
Phone | +1(800)526-4455 |
medical.services@crbard.com | |
Phone | +1(800)526-4455 |
medical.services@crbard.com | |
Phone | +1(800)526-4455 |
medical.services@crbard.com | |
Phone | +1(800)526-4455 |
medical.services@crbard.com | |
Phone | +1(800)526-4455 |
medical.services@crbard.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00801741219153 [Primary] |
GS1 | 10801741219150 [Package] Contains: 00801741219153 Package: CA [30 Units] In Commercial Distribution |
NZU | Collector, urine, powered, non indwelling catheter |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-08-09 |
Device Publish Date | 2022-08-01 |
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