Primary Device ID | 08714729019084 |
NIH Device Record Key | dfdebe47-2037-4e71-a06a-6eac744c3e95 |
Commercial Distribution Discontinuation | 2024-03-29 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | C-Flex™ Biliary |
Version Model Number | M00532020 |
Company DUNS | 021717889 |
Company Name | BOSTON SCIENTIFIC CORPORATION |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Safe |
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 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 | 08714729019084 [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 | 2024-04-03 |
Device Publish Date | 2015-09-24 |
08714729019121 | Biliary Stent |
08714729019114 | Biliary Stent |
08714729019107 | Biliary Stent |
08714729019091 | Biliary Stent |
08714729019084 | Biliary Stent |
08714729019077 | Biliary Stent |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
C-FLEX 90004192 not registered Live/Pending |
TADD, LLC 2020-06-16 |
C-FLEX 88207391 not registered Live/Pending |
The Nielsen Company (US), LLC 2018-11-27 |
C-FLEX 87480394 5807409 Live/Registered |
HÃBNER GmbH & Co. KG 2017-06-08 |
C-FLEX 86657802 not registered Dead/Abandoned |
Carolina Cap Company 2015-06-10 |
C-FLEX 86306725 4671430 Live/Registered |
Saint-Gobain Performance Plastics Corporation 2014-06-11 |
C-FLEX 85202859 3997488 Live/Registered |
Allen Medical Systems, Inc. 2010-12-21 |
C-FLEX 81014707 1014707 Dead/Cancelled |
Seeman Plastics, Incorporated 0000-00-00 |
C-FLEX 79379766 not registered Live/Pending |
SAFILO - Societa Azionaria Fabbrica Italiana Lavorazione Occhiali S.p.A. 2023-07-10 |
C-FLEX 78810285 3715311 Live/Registered |
Rayner Intraocular Lenses Limited 2006-02-08 |
C-FLEX 77675146 4060387 Live/Registered |
Pan-Oston Co. 2009-02-20 |
C-FLEX 77124230 3931252 Dead/Cancelled |
Colortronic Systems AG 2007-03-07 |
C-FLEX 77062166 3274079 Live/Registered |
Caravan Beads, Inc. 2006-12-12 |