Jostra AG

Also registered as Jostra AB

Country not established

Devices: 14

What Jostra AG makes

Jostra AG manufactures medical devices for cardiovascular perfusion and cardiothoracic surgery, including arterial perfusion cannulae, venous return catheters, cardiotomy reservoirs, and hollow fiber membrane oxygenators. Their portfolio also covers retrograde cardioplegia cannulae, vent catheters, flow probes, and suction devices designed for use in extracorporeal circulation systems.

The company’s devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. Jostra AG operates from the United States, with its products authorised for use in the US market.

AI-generated from registry data, 1 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue14

Newest first, rows 1-14 of 14

Search and filter all 14 devices

Jostra Arterial Perfusion Cannulae, Model A... Ref K012617

Class II

Active 510(k) 510(k) II
Heater Cooler Unit, Model Hcu 30 Ref K031544

Class II

Active 510(k) 510(k) II
Jostra Vent Catheters, Models Lv & Hkv Ref K022022

Class II

Active 510(k) 510(k) II
Els Cannula (Kit), Model M1210-88, M1510-88 Ref K002857

Class II

Active 510(k) 510(k) II
Quandrox Safeline Hollow Fiber Membrane Oxygenator, Model Hmo 2030 Ref K030264

Class II

Active 510(k) 510(k) II
Jostra Mecc System Ref K023132

Class II

Active 510(k) 510(k) II
Jostra Flowprobe Fp-32E Ref K013939

Class II

Active 510(k) 510(k) II
Jostra Suckers, Model Js Ref K020983

Class II

Active 510(k) 510(k) II
Jostra Dual Stage Venous Return Cannulae Ref K013944

Class II

Active 510(k) 510(k) II
Jostra Retrograde Cardioplegia Cannulae Ref K014303

Class II

Active 510(k) 510(k) II
Venous Hardshell Cardiotomy Resevoir, Model Vhk 4201 Ref K003551

Class II

Active 510(k) 510(k) II
Jostra Single Stage Venous Return Catheters Ref K020784

Class II

Active 510(k) 510(k) II
Jostra Arterial Perfusion Cannulae Ref K012774

Class II

Active 510(k) 510(k) II
Jostra Antegrade Cardioplegia Cannula Ref K020515

Class II

Active 510(k) 510(k) II

Rows 1-14 of 14

Frequently asked questions

How many devices does Jostra AG have in the registry?

The registry currently lists 14 devices for Jostra AG. Devices recorded under merged duplicate company entries are counted once.

Which registries list Jostra AG's devices?

Among its 14 most recently registered devices, Jostra AG has devices listed in FDA 510(k) (14 devices).

What risk classes do Jostra AG's devices fall under?

Among its 14 most recently registered devices, the classes recorded for Jostra AG's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Jostra AG in the registry?

The most recently registered devices listed for Jostra AG include JOSTRA ARTERIAL PERFUSION CANNULAE, MODEL A..., HEATER COOLER UNIT, MODEL HCU 30, JOSTRA VENT CATHETERS, MODELS LV & HKV and ELS CANNULA (KIT), MODEL M1210-88, M1510-88.

Generated automatically from registry data and not verified by a human reviewer.

What Jostra AG makes

Catalogue14

Jostra Arterial Perfusion Cannulae, Model A... Ref K012617

Heater Cooler Unit, Model Hcu 30 Ref K031544

Jostra Vent Catheters, Models Lv & Hkv Ref K022022

Els Cannula (Kit), Model M1210-88, M1510-88 Ref K002857

Quandrox Safeline Hollow Fiber Membrane Oxygenator, Model Hmo 2030 Ref K030264

Jostra Mecc System Ref K023132

Jostra Flowprobe Fp-32E Ref K013939

Jostra Suckers, Model Js Ref K020983

Jostra Dual Stage Venous Return Cannulae Ref K013944

Jostra Retrograde Cardioplegia Cannulae Ref K014303

Venous Hardshell Cardiotomy Resevoir, Model Vhk 4201 Ref K003551

Jostra Single Stage Venous Return Catheters Ref K020784

Jostra Arterial Perfusion Cannulae Ref K012774

Jostra Antegrade Cardioplegia Cannula Ref K020515

Frequently asked questions