Blueprint Genetics Oy
FI-MF-000009837 · Finland · Espoo
Blueprint Genetics Oy is registered in the European database on medical devices as a manufacturer, with 8 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Devices declared under this manufacturer
- Blueprint Genetics WES Platform – Family Seq
- Blueprint Genetics WES Platform – Family Seq + mtDNA Seq
- Blueprint Genetics WES Platform – Other Family Seq
- Blueprint Genetics WES Platform – Other Family Seq + mtDNA Seq
- Blueprint Genetics WES Platform – Proband + mtDNA Seq
- Blueprint Genetics WES Platform – Proband Seq
- Blueprint Genetics WES Platform – Variant Seq
- Blueprint Genetics WES Platform – Variant Seq + mtDNA Variant Seq
Catalogue references include WES-101, WES-102, WES-103, WES-104, WES-105, WES-106.
European nomenclature codes declared: W0106010199.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 8 |
| Country of registration | Finland |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 8 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Not found in the Canadian register |
|---|
⚠️ Canada lists no Class I devices at all — what that excludes.
North American profile: Neither register. Blueprint Genetics Oy was not found in either the U.S. or the Canadian register.