Advanced Practical Diagnostics
BE-MF-000000572 · Belgium · Turnhout
Advanced Practical Diagnostics is registered in the European database on medical devices as a manufacturer, with 10 devices declared. It has a similarly named entry in the FDA register that we have not verified.
What this manufacturer declares
Most frequent device types declared: 710001, 710101, 710201, 710301, 710401.
Devices declared under this manufacturer
- Adalimumab ELISA
- Anti-Adalimumab ELISA
- Anti-Infliximab ELISA
- Golimumab ELISA
- Infliximab ELISA
- MAIPA Assay
- Secukinumab ELISA
- Ustekinumab ELISA
- Vedolizumab ELISA
Catalogue references include 710001, 710201, 710301, 710401, 710501, 710701.
European nomenclature codes declared: W0102080799, W010399, W0102080702, W0102080701.
United States market access
| FDA establishment register | Similar name found — unverified |
|---|---|
| Matched entry | Advanced Cell Diagnostics, Inc. (US) · FDA 3009161685 |
| Devices in EUDAMED | 10 |
| Country of registration | Belgium |
⚠️ A similar name exists; we do not assert it is the same company — why.
Device-level evidence
| Devices with a numeric GTIN | 10 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Similar name found — unverified |
|---|---|
| Matched entry | ADVANCED MEDICAL DIAGNOSTICS SA/NV |
⚠️ A similar name exists; unverified — why.