Primary Device ID | 08714729296881 |
NIH Device Record Key | 5b3fbca3-8b3b-40bb-ac94-c3b15f500ea7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | WALLSTENT™ RX BILIARY |
Version Model Number | M00569680 |
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 | 08714729296881 [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 |