Phadia AB
SE-MF-000014170 · Sweden · Uppsala
Phadia AB is registered in the European database on medical devices as a manufacturer, with 802 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
Devices declared under this manufacturer
- Dilution Plate, Phadia 250
- EliA ASCA IgG Well
- EliA PR3S Well
- ImmunoCAP Allergen c202, Suxamethonium (Succinylcholine)
- ImmunoCAP Allergen d2, House dust mite
- ImmunoCAP Allergen e1, Cat dander
- ImmunoCAP Allergen e231, Allergen component rFel d 7 Cat
- ImmunoCAP Allergen f201, Pecan nut
- ImmunoCAP Allergen f424, Allergen component rAra h 3 Peanut
- ImmunoCAP Allergen f425, Allergen component rCor a 8, Hazel nut
- ImmunoCAP Allergen f432, Allergen component nGly m 6 Glycinin, Soy
- ImmunoCAP Allergen g211, Allergen component rPhl p 11 Timothy
Showing 12 of 802 declared devices.
Catalogue references include 14-4109-01, 14-4807-01, 14-4965-01, 14-4968-01, 14-4991-01, 14-5266-01.
European nomenclature codes declared: W01020202, W0102152011, W01029003, W0102010105, W0102152099, W0102019009.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | PHADIA GMBH (DE) · FDA 9680745 |
| Devices in EUDAMED | 802 |
| Country of registration | Sweden |
Device-level evidence
| Devices with a numeric GTIN | 802 |
|---|---|
| Found in the U.S. device database | 494 |
| Share | 61.6 % |
Canadian market access
| Health Canada licence listing | Licensed in Canada |
|---|---|
| Matched entry | PHADIA GMBH |
North American profile: Both markets. Phadia AB is registered in both the United States and Canada.