| Primary Device ID | 10801741052221 |
| NIH Device Record Key | eb6776a6-d9f2-49dc-af53-2386cbaad045 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Bardia® Piston Syringe |
| Version Model Number | 802065 |
| Catalog Number | 802065 |
| 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 | true |
| OTC Over-The-Counter | false |
| Phone | +1(800)526-4455 |
| medical.services@crbard.com | |
| Phone | +1(800)526-4455 |
| medical.services@crbard.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00801741052224 [Primary] |
| GS1 | 10801741052221 [Package] Contains: 00801741052224 Package: BX [25 Units] In Commercial Distribution |
| GS1 | 20801741052228 [Package] Package: CA [2 Units] In Commercial Distribution |
| KYZ | SYRINGE, IRRIGATING (NON DENTAL) |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2016-12-19 |
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| 10801741226967 - PureWick | 2024-08-06 PureWick Flex Female External Catheter, Acute Care |
| 10801741226981 - PureWick | 2024-08-06 PureWick Flex Female External Catheter, Home Care |
| 10801741226462 - PureWick | 2024-06-10 PureWick Male External Catheter, Home Care |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() BARDIA 74031475 1633098 Live/Registered |
C.R. Bard, Inc. 1990-02-22 |