Primary Device ID | 08714729035886 |
NIH Device Record Key | ffb4fcd4-2078-4446-8ea6-e06239e0c98e |
Commercial Distribution Discontinuation | 2023-02-07 |
Commercial Distribution Status | Not in Commercial Distribution |
Version Model Number | M001465500 |
Company DUNS | 021717889 |
Company Name | BOSTON SCIENTIFIC CORPORATION |
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 | 08714729035886 [Package] Contains: 08714729741404 Package: [12 Units] Discontinued: 2023-02-07 Not in Commercial Distribution |
GS1 | 08714729741404 [Primary] |
OCY | Endoscopic guidewire, gastroenterology-urology |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2025-03-11 |
Device Publish Date | 2016-09-24 |
00191506044466 - WallFlex™ | 2025-03-11 Stent System |
00191506044473 - WallFlex™ | 2025-03-11 Stent System |
00191506044480 - WallFlex™ | 2025-03-11 Stent System |
00191506044497 - WallFlex™ | 2025-03-11 Stent System |
00191506044503 - WallFlex™ | 2025-03-11 Stent System |
00191506044510 - WallFlex™ | 2025-03-11 Stent System |
00191506044527 - WallFlex™ | 2025-03-11 Stent System |
08714729035886 - NA | 2025-03-11Torque Vise |
08714729035886 - NA | 2025-03-11 Torque Vise |