Primary Device ID | 08717648344251 |
NIH Device Record Key | 89a14d02-41ad-4d8d-b965-76887e2bb6f0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Supera™ |
Version Model Number | S-70-040-120-P6 |
Catalog Number | S-70-040-120-P6 |
Company DUNS | 964569052 |
Company Name | ABBOTT VASCULAR INC. |
Device Count | 1 |
DM Exempt | true |
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 |
Stent Length | 40 Millimeter |
Stent Diameter | 7 Millimeter |
Stent Length | 40 Millimeter |
Stent Diameter | 7 Millimeter |
Stent Length | 40 Millimeter |
Stent Diameter | 7 Millimeter |
Stent Length | 40 Millimeter |
Stent Diameter | 7 Millimeter |
Stent Length | 40 Millimeter |
Stent Diameter | 7 Millimeter |
Stent Length | 40 Millimeter |
Stent Diameter | 7 Millimeter |
Stent Length | 40 Millimeter |
Stent Diameter | 7 Millimeter |
Stent Length | 40 Millimeter |
Stent Diameter | 7 Millimeter |
Stent Length | 40 Millimeter |
Stent Diameter | 7 Millimeter |
Stent Length | 40 Millimeter |
Stent Diameter | 7 Millimeter |
Stent Length | 40 Millimeter |
Stent Diameter | 7 Millimeter |
Stent Length | 40 Millimeter |
Stent Diameter | 7 Millimeter |
Stent Length | 40 Millimeter |
Stent Diameter | 7 Millimeter |
Stent Length | 40 Millimeter |
Stent Diameter | 7 Millimeter |
Stent Length | 40 Millimeter |
Stent Diameter | 7 Millimeter |
Stent Length | 40 Millimeter |
Stent Diameter | 7 Millimeter |
Stent Length | 40 Millimeter |
Stent Diameter | 7 Millimeter |
Stent Length | 40 Millimeter |
Stent Diameter | 7 Millimeter |
Stent Length | 40 Millimeter |
Stent Diameter | 7 Millimeter |
Stent Length | 40 Millimeter |
Stent Diameter | 7 Millimeter |
Stent Length | 40 Millimeter |
Stent Diameter | 7 Millimeter |
Stent Length | 40 Millimeter |
Stent Diameter | 7 Millimeter |
Stent Length | 40 Millimeter |
Stent Diameter | 7 Millimeter |
Stent Length | 40 Millimeter |
Stent Diameter | 7 Millimeter |
Stent Length | 40 Millimeter |
Stent Diameter | 7 Millimeter |
Stent Length | 40 Millimeter |
Stent Diameter | 7 Millimeter |
Stent Length | 40 Millimeter |
Stent Diameter | 7 Millimeter |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from Direct Sunlight,Keep Dry. |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from Direct Sunlight,Keep Dry. |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from Direct Sunlight,Keep Dry. |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from Direct Sunlight,Keep Dry. |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from Direct Sunlight,Keep Dry. |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from Direct Sunlight,Keep Dry. |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from Direct Sunlight,Keep Dry. |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from Direct Sunlight,Keep Dry. |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from Direct Sunlight,Keep Dry. |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from Direct Sunlight,Keep Dry. |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from Direct Sunlight,Keep Dry. |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from Direct Sunlight,Keep Dry. |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from Direct Sunlight,Keep Dry. |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from Direct Sunlight,Keep Dry. |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from Direct Sunlight,Keep Dry. |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from Direct Sunlight,Keep Dry. |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from Direct Sunlight,Keep Dry. |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from Direct Sunlight,Keep Dry. |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from Direct Sunlight,Keep Dry. |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from Direct Sunlight,Keep Dry. |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from Direct Sunlight,Keep Dry. |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from Direct Sunlight,Keep Dry. |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from Direct Sunlight,Keep Dry. |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from Direct Sunlight,Keep Dry. |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from Direct Sunlight,Keep Dry. |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from Direct Sunlight,Keep Dry. |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from Direct Sunlight,Keep Dry. |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from Direct Sunlight,Keep Dry. |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from Direct Sunlight,Keep Dry. |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from Direct Sunlight,Keep Dry. |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from Direct Sunlight,Keep Dry. |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from Direct Sunlight,Keep Dry. |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from Direct Sunlight,Keep Dry. |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from Direct Sunlight,Keep Dry. |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from Direct Sunlight,Keep Dry. |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from Direct Sunlight,Keep Dry. |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08717648344251 [Primary] |
NIP | STENT, SUPERFICIAL FEMORAL ARTERY |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-09-02 |
Device Publish Date | 2021-08-25 |
08717648350627 | Supera™ Peripheral Stent System 7.0 mm x 100 mm x 120 cm 6 F |
08717648344275 | Supera™ Peripheral Stent System 7.0 mm x 80 mm x 120 cm 6 F |
08717648344268 | Supera™ Peripheral Stent System 7.0 mm x 60 mm x 120 cm 6 F |
08717648344251 | Supera™ Peripheral Stent System 7.0 mm x 40 mm x 120 cm 6 F |
08717648344244 | Supera™ Peripheral Stent System 7.0 mm x 30 mm x 120 cm 6 F |
08717648344237 | Supera™ Peripheral Stent System 7.0 mm x 20 mm x 120 cm 6 F |
08717648294501 | Supera™ Peripheral Stent System 7.5 mm x 100 mm x 120 cm 6 F |
08717648294495 | Supera™ Peripheral Stent System 7.5 mm x 80 mm x 120 cm 6 F |
08717648294488 | Supera™ Peripheral Stent System 7.5 mm x 60 mm x 120 cm 6 F |
08717648294471 | Supera™ Peripheral Stent System 7.5 mm x 40 mm x 120 cm 6 F |
08717648294464 | Supera™ Peripheral Stent System 7.5 mm x 30 mm x 120 cm 6 F |
08717648294457 | Supera™ Peripheral Stent System 7.5 mm x 20 mm x 120 cm 6 F |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
SUPERA 97678297 not registered Live/Pending |
Wahl GmbH 2022-11-15 |
SUPERA 90448750 not registered Live/Pending |
Pride Centric Resources, Inc. 2021-01-05 |
SUPERA 90448687 not registered Live/Pending |
Pride Centric Resources, Inc. 2021-01-05 |
SUPERA 88686541 not registered Live/Pending |
Superior Glove Works Ltd. 2019-11-10 |
SUPERA 88439071 not registered Live/Pending |
Huang, Weifeng 2019-05-21 |
SUPERA 88434675 not registered Live/Pending |
Huang, Weifeng 2019-05-17 |
SUPERA 86295560 not registered Dead/Abandoned |
Paul Koester 2014-05-29 |
SUPERA 85950119 4672477 Live/Registered |
Supera, LLC 2013-06-04 |
SUPERA 85766456 4689113 Live/Registered |
Oxiquimica Agrociencia Ltda. 2012-10-29 |
SUPERA 79383088 not registered Live/Pending |
Ramazan Barlas 2023-08-03 |
SUPERA 78917486 3455712 Live/Registered |
IDev Technologies, Inc. 2006-06-27 |
SUPERA 78276113 not registered Dead/Abandoned |
KORD Beteiligungsgesellschaft mbH & Co.KG 2003-07-18 |