Primary Device ID | 07640142811848 |
NIH Device Record Key | 8a3f925d-cbc5-4ac7-b0c9-c0d919c63282 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Rotarex™S 8 F x 110 cm |
Version Model Number | 80335 |
Catalog Number | 80335 |
Company DUNS | 488489766 |
Company Name | Straub Medical AG |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
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 |
Phone | +41817200460 |
info@straubmedical.com | |
Phone | +41817200460 |
info@straubmedical.com | |
Phone | +41817200460 |
info@straubmedical.com | |
Phone | +41817200460 |
info@straubmedical.com | |
Phone | +41817200460 |
info@straubmedical.com | |
Phone | +41817200460 |
info@straubmedical.com | |
Phone | +41817200460 |
info@straubmedical.com | |
Phone | +41817200460 |
info@straubmedical.com | |
Phone | +41817200460 |
info@straubmedical.com | |
Phone | +41817200460 |
info@straubmedical.com | |
Phone | +41817200460 |
info@straubmedical.com | |
Phone | +41817200460 |
info@straubmedical.com | |
Phone | +41817200460 |
info@straubmedical.com | |
Phone | +41817200460 |
info@straubmedical.com | |
Phone | +41817200460 |
info@straubmedical.com | |
Phone | +41817200460 |
info@straubmedical.com | |
Phone | +41817200460 |
info@straubmedical.com | |
Phone | +41817200460 |
info@straubmedical.com | |
Phone | +41817200460 |
info@straubmedical.com | |
Phone | +41817200460 |
info@straubmedical.com | |
Phone | +41817200460 |
info@straubmedical.com | |
Phone | +41817200460 |
info@straubmedical.com | |
Phone | +41817200460 |
info@straubmedical.com | |
Phone | +41817200460 |
info@straubmedical.com | |
Phone | +41817200460 |
info@straubmedical.com |
Catheter Gauge | 8 French |
Catheter Working Length | 110 Centimeter |
Catheter Gauge | 8 French |
Catheter Working Length | 110 Centimeter |
Catheter Gauge | 8 French |
Catheter Working Length | 110 Centimeter |
Catheter Gauge | 8 French |
Catheter Working Length | 110 Centimeter |
Catheter Gauge | 8 French |
Catheter Working Length | 110 Centimeter |
Catheter Gauge | 8 French |
Catheter Working Length | 110 Centimeter |
Catheter Gauge | 8 French |
Catheter Working Length | 110 Centimeter |
Catheter Gauge | 8 French |
Catheter Working Length | 110 Centimeter |
Catheter Gauge | 8 French |
Catheter Working Length | 110 Centimeter |
Catheter Gauge | 8 French |
Catheter Working Length | 110 Centimeter |
Catheter Gauge | 8 French |
Catheter Working Length | 110 Centimeter |
Catheter Gauge | 8 French |
Catheter Working Length | 110 Centimeter |
Catheter Gauge | 8 French |
Catheter Working Length | 110 Centimeter |
Catheter Gauge | 8 French |
Catheter Working Length | 110 Centimeter |
Catheter Gauge | 8 French |
Catheter Working Length | 110 Centimeter |
Catheter Gauge | 8 French |
Catheter Working Length | 110 Centimeter |
Catheter Gauge | 8 French |
Catheter Working Length | 110 Centimeter |
Catheter Gauge | 8 French |
Catheter Working Length | 110 Centimeter |
Catheter Gauge | 8 French |
Catheter Working Length | 110 Centimeter |
Catheter Gauge | 8 French |
Catheter Working Length | 110 Centimeter |
Catheter Gauge | 8 French |
Catheter Working Length | 110 Centimeter |
Catheter Gauge | 8 French |
Catheter Working Length | 110 Centimeter |
Catheter Gauge | 8 French |
Catheter Working Length | 110 Centimeter |
Catheter Gauge | 8 French |
Catheter Working Length | 110 Centimeter |
Catheter Gauge | 8 French |
Catheter Working Length | 110 Centimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07640142811848 [Primary] |
MCW | Catheter, Peripheral, Atherectomy |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-05-12 |
Device Publish Date | 2022-05-04 |
07640142810407 - Aspirex® S 6F 110 cm | 2022-07-08 The Aspirex® S catheter (gauge 6F; length 110cm) is over-the-wire, single use, percutaneous device for the treatment of occlusi |
07640142810438 - Aspirex® S 6F 135cm | 2022-07-08 The Aspirex® S catheter (gauge 6F; length 135cm) is over-the-wire, single use, percutaneous device for the treatment of occlusi |
07640142810452 - Aspirex® S 8F 85cm | 2022-07-08 The Aspirex® S catheter (gauge 8F; length 85cm) is over-the-wire, single use, percutaneous device for the treatment of occlusio |
07640142810483 - Aspirex® S 8F 110cm | 2022-07-08 The Aspirex® S catheter (gauge 8F; length 110cm) is over-the-wire, single use, percutaneous device for the treatment of occlusi |
07640142810506 - Aspirex® S 10F 110cm | 2022-07-08 The Aspirex® S catheter (gauge 10F; length 110cm) is over-the-wire, single use, percutaneous device for the treatment of occlus |
07640142810735 - Guidewire 0.025 6/270cm angled | 2022-07-08 The Rotarex™ S and Aspirex™ S Guidewire has a LubriSkin PTFE-coated nitinol core wire with a gold-plated Tungsten tip coated |
07640142811312 - SET Aspirex™ S 6F 110cm | 2022-07-08 The Aspirex™ S Thrombectomy Catheter Set is composed of one Aspirex™ S Thrombectomy Catheter (gauge 6F; length 110cm), one A |
07640142811329 - SET Aspirex™ S 6F 135cm | 2022-07-08 The Aspirex™ Thrombectomy Catheter Set is composed of one Aspirex™ Thrombectomy Catheter (gauge 6F; length 135cm), one Aspir |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ROTAREX 79233933 5759861 Live/Registered |
LUXEMBOURG PATENT COMPANY S.A. 2017-12-20 |
ROTAREX 79055967 3728503 Live/Registered |
Straub Medical AG 2008-05-06 |
ROTAREX 75859948 2557769 Live/Registered |
Straub Medical AG 1999-11-29 |
ROTAREX 73084406 1134985 Dead/Cancelled |
EX-CELL-O GMBH 1978-08-24 |