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Rossix AB

Active in EUDAMED

Swedenfrom SRN EUDAMED FDA SRN SE-MF-000027429 FEI 3004075036

Devices
1
Registrations
EUDAMEDFDA
FDA recalls
0

At a glance

Counted by deviCERTS from registry records

Market reach

European Union
EUDAMED actor
United States
FDA FEI

Catalogue1

Newest first, rows 1-1 of 1

  • Rox Factor IX Ref 900020

    Withdrawn Regimes: CE IVDD, withdrawn Registry: EUDAMED Class:IVD General

Company details

EUDAMED SRN
SE-MF-000027429
FDA FEI number
3004075036
EU VAT number
SE556830318301
EUDAMED status
Active
EUDAMED registered name
Rossix AB
EUDAMED abbreviated name
Rossix
Registered address
3B, Taljegårdsgatan, 431 53, Mölndal, Sweden
Phone
+46 31 7068965
PRRC contact
Pia Bryngelhed(public in EUDAMED)

From the company website

Read 18 Sep 2026

Rossix provides products for use in hemostasis and thrombosis research and our laboratory is able to handle a broad range of Contract Analyses.

From the manufacturer's own website. Source

Frequently asked questions

How many devices does Rossix AB have in the registry?

The registry currently lists 1 device for Rossix AB. Devices recorded under merged duplicate company entries are counted once.

Which registries list Rossix AB's devices?

Among its 1 most recently registered device, Rossix AB has devices listed in EUDAMED (1 device).

What risk classes do Rossix AB's devices fall under?

Among its 1 most recently registered device, the classes recorded for Rossix AB's devices are IVD general. Each device page shows its own class and authorisation.

What are the newest devices from Rossix AB in the registry?

The most recently registered devices listed for Rossix AB include Rox Factor IX.

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