| Primary Device ID | 10801741113908 |
| NIH Device Record Key | 02577b48-b79d-4015-a0b2-f0949b0c290b |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Bard® Lopez Valve® with ENFit™ |
| Version Model Number | EN0056000 |
| Catalog Number | EN0056000 |
| Company DUNS | 016898496 |
| Company Name | C. R. Bard, Inc. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| 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 | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00801741113901 [Primary] |
| GS1 | 10801741113908 [Package] Contains: 00801741113901 Package: CA [50 Units] In Commercial Distribution |
| KNT | TUBES, GASTROINTESTINAL (AND ACCESSORIES) |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-11-22 |
| 10801741127653 - Bard® X-Force® Nephrostomy Balloon Dilation Catheter | 2025-08-05 Bard® X-Force® Nephrostomy Balloon Dilation Catheter |
| 10801741127660 - Bard® X-Force® Nephrostomy Balloon Dilation Catheter | 2025-08-05 Bard® X-Force® Nephrostomy Balloon Dilation Catheter |
| 10801741011655 - Bard® Silicone Uretero-Intestinal Anastomosis Urinary Diversion Stent | 2025-04-25 Bard® Silicone Uretero-Intestinal Anastomosis Urinary Diversion Stent with Hydro-Glide™ Guidewire |
| 10801741171809 - Bardia | 2025-03-18 Bardia Silicone Elastomer Coated Foley Catheter |
| 10801741171816 - Bardia | 2025-03-18 Bardia Silicone Elastomer Coated Foley Catheter |
| 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 |
|---|---|
![]() BARD 97907417 not registered Live/Pending |
XTRM Gears LLC 2023-04-26 |
![]() BARD 97819147 not registered Live/Pending |
Library of Congress 2023-03-02 |
![]() BARD 97780614 not registered Live/Pending |
Google LLC 2023-02-03 |
![]() BARD 97173545 not registered Live/Pending |
Bard College 2021-12-15 |
![]() BARD 86982669 5476077 Live/Registered |
C. R. Bard, Inc. 2015-05-26 |
![]() BARD 86593150 4858616 Live/Registered |
C. R. Bard, Inc. 2015-04-10 |
![]() BARD 85144625 not registered Dead/Abandoned |
Luke Christenson 2010-10-04 |
![]() BARD 85144625 not registered Dead/Abandoned |
Steven Crandall 2010-10-04 |
![]() BARD 85144625 not registered Dead/Abandoned |
Jacob Craner 2010-10-04 |
![]() BARD 85015955 3873568 Live/Registered |
C. R. Bard, Inc. 2010-04-16 |
![]() BARD 78296485 not registered Dead/Abandoned |
MATTEL, INC. 2003-09-05 |
![]() BARD 76070857 not registered Dead/Abandoned |
Tvornica duhana Rovinj 2000-06-14 |