Straub Medical AG

Address:Straubstrasse 12,Wangs Sankt Gallen,CH

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Premarket Exempt
Clear

Device Description : The plastic sleeve is used to cover and keep the handle/motor or footswitch clea The plastic sleeve is used to cover and keep the handle/motor or footswitch clean and allows the motor to enter the sterile field.

Device Class : 2

Duns Number: 488489766

Premarket Exempt : No

Product Code : KKX

Prescription Use : Yes

Device Count : 1

Device Description : The Rotarex™ S and Aspirex™ S Guidewire has a LubriSkin PTFE-coated nitinol core The Rotarex™ S and Aspirex™ S Guidewire has a LubriSkin PTFE-coated nitinol core wire with a gold-plated Tungsten tip coated with DSM ComfortCoat® hydrophilic coating. The guidewire is used to initially cross through the area to be treated. To be used with Straub Medical catheters.

Device Class :

Duns Number: 488489766

Premarket Exempt : No

Product Code : DQX

Prescription Use : Yes

Device Count : 1

Device Description : The Rotarex™ S and Aspirex™ S Guidewire has a LubriSkin PTFE-coated nitinol core The Rotarex™ S and Aspirex™ S Guidewire has a LubriSkin PTFE-coated nitinol core wire with a gold-plated Tungsten tip coated with DSM ComfortCoat® hydrophilic coating. The guidewire is used to initially cross through the area to be treated. To be used with Straub Medical catheters.

Device Class :

Duns Number: 488489766

Premarket Exempt : No

Product Code : DQX

Prescription Use : Yes

Device Count : 1

Device Description : The Rotarex™ S and Aspirex™ S Guidewire has a LubriSkin PTFE-coated nitinol core The Rotarex™ S and Aspirex™ S Guidewire has a LubriSkin PTFE-coated nitinol core wire with a gold-plated Tungsten tip coated with DSM ComfortCoat® hydrophilic coating. The guidewire is used to initially cross through the area to be treated. To be used with Straub Medical catheters.

Device Class :

Duns Number: 488489766

Premarket Exempt : No

Product Code : DQX

Prescription Use : Yes

Device Count : 1

Device Description : The Rotarex®S catheter (gauge 6F; length 110 cm) is over-the-wire, single use, p The Rotarex®S catheter (gauge 6F; length 110 cm) is over-the-wire, single use, percutaneous device for the treatment of occlusions in arterial vasculature.

Device Class : 2

Duns Number: 488489766

Premarket Exempt : No

Product Code : MCW

Prescription Use : Yes

Device Count : 1

Device Description : The Rotarex®S catheter (gauge 6F; length 135 cm) is over-the-wire, single use, p The Rotarex®S catheter (gauge 6F; length 135 cm) is over-the-wire, single use, percutaneous device for the treatment of occlusions in arterial vasculature.

Device Class : 2

Duns Number: 488489766

Premarket Exempt : No

Product Code : MCW

Prescription Use : Yes

Device Count : 1

Device Description : The Rotarex®S catheter (gauge 8F; length 85 cm) is over-the-wire, single use, pe The Rotarex®S catheter (gauge 8F; length 85 cm) is over-the-wire, single use, percutaneous device for the treatment of occlusions in arterial vasculature.

Device Class : 2

Duns Number: 488489766

Premarket Exempt : No

Product Code : MCW

Prescription Use : Yes

Device Count : 1

Device Description : The Rotarex®S catheter (gauge 8F; length 110 cm) is over-the-wire, single use, p The Rotarex®S catheter (gauge 8F; length 110 cm) is over-the-wire, single use, percutaneous device for the treatment of occlusions in arterial vasculature.

Device Class : 2

Duns Number: 488489766

Premarket Exempt : No

Product Code : MCW

Prescription Use : Yes

Device Count : 1

Device Description : The Aspirex® S catheter (gauge 6F; length 110cm) is over-the-wire, single use, p The Aspirex® S catheter (gauge 6F; length 110cm) is over-the-wire, single use, percutaneous device for the treatment of occlusions in venous vasculature.

Device Class : 2

Duns Number: 488489766

Premarket Exempt : No

Product Code : QEW

Prescription Use : Yes

Device Count : 1

Device Description : The Aspirex® S catheter (gauge 6F; length 135cm) is over-the-wire, single use, p The Aspirex® S catheter (gauge 6F; length 135cm) is over-the-wire, single use, percutaneous device for the treatment of occlusions in venous vasculature.

Device Class : 2

Duns Number: 488489766

Premarket Exempt : No

Product Code : QEW

Prescription Use : Yes

Device Count : 1