Primary Device ID | 00763000886714 |
NIH Device Record Key | fd754ec4-8ea6-41d7-9f0f-bb1ed74d42f3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | C-Flex |
Version Model Number | 1524075 |
Company DUNS | 835465063 |
Company Name | MEDTRONIC XOMED, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00763000886714 [Primary] |
LYA | SPLINT, INTRANASAL SEPTAL |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-07-01 |
Device Publish Date | 2025-06-23 |
00763000309480 - Causse/Polycel | 2025-07-01 PROSTHESIS 1156376 CAUSSE FLPL PARTIAL |
20763000870359 - Microgel | 2025-07-01 VENT TUBE 1082201 5PK PAPA TYPE 1.14 |
20763000870366 - Sheehy | 2025-07-01 VENT TUBE 1083301 5PK SHEEHY TYPE 1.27 |
20763000870373 - 20763000870373 | 2025-07-01 VENT TUBE 1084401 5PK GROMMET 1.27 |
20763000870380 - Reuter | 2025-07-01 VENT TUBE 1010201 5PK BOBBIN 1.14 FLPL |
20763000870403 - Sheehy | 2025-07-01 VENT TUBE 1013301 5PK BUTTON 1.27 FLPL |
20763000870410 - Donaldson | 2025-07-01 VENT TUBE 1015101 5PK DONLDSN 1.14 FLPL |
20763000870427 - Shepard | 2025-07-01 VENT TUBE 1016101 5PK GROMMET 1.14 FLPL |
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 |