Apriomed AB
Active in EUDAMEDSwedenfrom SRN EUDAMED FDA SRN SE-MF-000001013 FEI 3007664053
Apriomed AB is a medical device manufacturer based in Sweden, with 80 devices listed in FDA GUDID, EUDAMED and FDA 510(k) (EU Class IIa and I; FDA Class II and I) as of 14 Nov 2026.
- Devices
- 80
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
Registry facts
- Registries
- FDA GUDID 71
- EUDAMED 48
- FDA 510(k) 2
- Device classes
- EU Class IIa 42
- FDA Class II 17
- FDA Class I 15
- EU Class I 6
- Top EMDN categories
- Needles 48
- Identifiers
- EUDAMED SRN SE-MF-000001013
- FDA FEI 3007664053
- DUNS 631734758
At a glance
Market reach
- European Union
- EUDAMED actor
- United States
- FDA FEI
Catalogue
Search and filter all 80 devicesShowing 1-50 of 80
Company details
- EUDAMED SRN
- SE-MF-000001013
- FDA FEI number
- 3007664053
- DUNS number
- 631734758
- EU VAT number
- SE556581924901
- EUDAMED status
- Active
- EUDAMED registered name
- AprioMed AB
- Registered address
- 28, Virdings Allé, 754 50, Uppsala, Sweden
- info@apriomed.com
- Phone
- +46184301440
- PRRC contact
- Katrin Svensson
Frequently asked questions
How many devices does Apriomed AB have in the registry?
The registry currently lists 80 devices for Apriomed AB. Devices recorded under merged duplicate company entries are counted once.
Which registries list Apriomed AB's devices?
Among its 50 most recently registered devices, Apriomed AB has devices listed in EUDAMED (18 devices), FDA 510(k) (2 devices) and FDA GUDID (45 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Apriomed AB's devices fall under?
Among its 50 most recently registered devices, the classes recorded for Apriomed AB's devices are Class I, Class IIa and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Apriomed AB in the registry?
The most recently registered devices listed for Apriomed AB include Gangi-SoftGuard Coaxial Needle SG15-071, SeeStar 13312, Gangi-HydroGuard Coaxial Needle HG17-121 and Bonopty Biopsy Set 10-1063.