Primary Device ID | 08714729759256 |
NIH Device Record Key | 51ae4f98-b412-4929-b1e8-7cdc612caf98 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | WallFlex™ Biliary |
Version Model Number | M00570610 |
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 Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08714729759256 [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 | 2022-04-08 |
Device Publish Date | 2015-09-24 |
08714729764922 | WALLFLEX BILIARY RX COVERED 10X80 |
08714729764915 | WALLFLEX BILIARY RX COVERED 10X60 |
08714729764908 | WALLFLEX BILIARY RX COVERED 10X40 |
08714729764892 | WALLFLEX BILIARY RX COVERED 8X80 |
08714729764885 | WALLFLEX BILIARY RX COVERED 8X60 |
08714729759331 | Stent System |
08714729759324 | Stent System |
08714729759317 | Stent System |
08714729759300 | Stent System |
08714729759294 | Stent System |
08714729765332 | Stent System |
08714729759287 | Stent System |
08714729759270 | Stent System |
08714729759263 | Stent System |
08714729759256 | Stent System |
08714729759249 | Stent System |
08714729758150 | Stent System |
08714729756231 | Stent System |
00191506026226 | RX Fully Covered Stent System |
00191506026202 | RX Fully Covered Stent System |
00191506026189 | RX Partially Covered Stent System |
00191506026165 | RX Partially Covered Stent System |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
WALLFLEX 78408742 3121616 Live/Registered |
BOSTON SCIENTIFIC SCIMED, INC. 2004-04-27 |