Aidian Oy
Active in EUDAMEDFinlandfrom SRN EUDAMED FDA SRN FI-MF-000023611 FEI 3002807786
Aidian Oy is a medical device manufacturer based in Finland, with 77 devices listed in EUDAMED and FDA GUDID (EU IVD General and Class A; FDA Class I) as of 14 Nov 2026.
- Devices
- 77
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
Registry facts
- Registries
- EUDAMED 72
- FDA GUDID 10
- Device classes
- EU IVD General 59
- EU Class A 13
- FDA Class I 5
- Top EMDN categories
- Identifiers
- EUDAMED SRN FI-MF-000023611
- FDA FEI 3002807786
- DUNS 401656868
At a glance
EU certificates
1 of 1 in force.
Market reach
- European Union
- EUDAMED actor, 1 certificate
- United States
- FDA FEI
What Aidian Oy makes
Aidian Oy manufactures in vitro diagnostic (IVD) products including multiple formulation agar culture media for microbiological testing, reagents for apolipoprotein B (Apo B) and human immunoglobulin G (IgG) animal conjugate antibody detection, and photometric/spectroscopic immunoassay analysers. Specific devices include the QuikRead go® Instrument and QuikRead go Plus Instrument, Uricult® culture media variants (such as CLED/MacConkey, CLED/EMB, and CLED+Polymyxin formulations), UniQ PINP RIA assay, and various QuikRead go controls for hemoglobin and C-reactive protein testing.
The company's IVD portfolio is classified as Class A, Class I, and IVD General under regulatory frameworks, and its devices are listed in the EUDAMED and FDA UDI registries. Aidian Oy is based in Finland.
Catalogue
Search and filter all 77 devicesShowing 1-50 of 77
Company details
- EUDAMED SRN
- FI-MF-000023611
- FDA FEI number
- 3002807786
- DUNS number
- 401656868
- EU VAT number
- FI18552161
- EUDAMED status
- Active
- EUDAMED registered name
- Aidian Oy
- Registered address
- 6B, Koivu-Mankkaan tie, 02200, Espoo, Finland
- Website
- www.aidian.eu/
- eudamed@aidian.eu
- Phone
- +358 10 309 3000
- PRRC contact
- Rina Wahlroos
EUDAMED certificates
1 certificate1 valid, 0 expiredIVDR 1next expiry 14 Aug 2029
TÜV SÜD Product Service GmbH 0123 1 certificate
- V74 091680 0004 Active
Technical documentation EU IVDR
- Issued
- 30 Jun 2026
- Expires
- 14 Aug 2029
- Reason
- Change approved
Frequently asked questions
How many devices does Aidian Oy have in the registry?
The registry currently lists 77 devices for Aidian Oy. Devices recorded under merged duplicate company entries are counted once.
Which registries list Aidian Oy's devices?
Among its 50 most recently registered devices, Aidian Oy has devices listed in EUDAMED (45 devices) and FDA GUDID (10 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Aidian Oy's devices fall under?
Among its 50 most recently registered devices, the classes recorded for Aidian Oy's devices are Class I, IVDR Class A and IVD general. Each device page shows its own class and authorisation.
What EUDAMED certificates are recorded for Aidian Oy?
EUDAMED lists 1 certificate for Aidian Oy (technical documentation) under IVDR. The most recent was issued on 30 Jun 2026.
What are the newest devices from Aidian Oy in the registry?
The most recently registered devices listed for Aidian Oy include QuikRead go® Instrument 145218, Uricult® CLED/MacConkey 68019, Uricult CLED/EMB 68014 and Uricult® CLED+Polymyxin / MacConkey 68017.