| Primary Device ID | 08714729296874 |
| NIH Device Record Key | 1159bb52-2eb9-47a5-b063-a8c794ab11f2 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | WALLSTENT™ RX BILIARY |
| Version Model Number | M00569670 |
| Company DUNS | 021717889 |
| Company Name | BOSTON SCIENTIFIC CORPORATION |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Conditional |
| 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 Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 08714729296874 [Primary] |
| FGE | CATHETER, BILIARY, DIAGNOSTIC |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2021-07-22 |
| Device Publish Date | 2015-09-24 |
| 08714729296911 | RX Biliary Endoprosthesis Stent System |
| 08714729296904 | RX Biliary Endoprosthesis Stent System |
| 08714729296898 | RX Biliary Endoprosthesis Stent System |
| 08714729296881 | RX Biliary Endoprosthesis Stent System |
| 08714729296928 | RX Biliary Endoprosthesis Stent System |
| 08714729296874 | RX Biliary Endoprosthesis Stent System |
| 08714729456728 | RX Biliary Endoprosthesis Stent System |
| 08714729456711 | RX Biliary Endoprosthesis Stent System |
| 08714729296867 | RX Biliary Endoprosthesis Stent System |
| 08714729296850 | RX Biliary Endoprosthesis Stent System |
| 08714729296843 | RX Biliary Endoprosthesis Stent System |
| 08714729296836 | RX Biliary Endoprosthesis Stent System |
| 08714729296829 | RX Biliary Endoprosthesis Stent System |
| 08714729296812 | RX Biliary Endoprosthesis Stent System |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() WALLSTENT 73713251 1539188 Live/Registered |
MEDINVENT S.A. 1988-02-25 |