Establishment registration
BIOSERENITY MEDICAL DEVICES GROUP
FDA establishment registration 3014027738 · PARIS CEDEX 13 Ile-de-France, FR
Key facts
| Registration number | 3014027738 |
|---|---|
| Establishment name | BIOSERENITY MEDICAL DEVICES GROUP |
| Owner/operator | BIOSERENITY MEDICAL DEVICES GROUP |
| Owner/operator number | 10089585 |
| FEI number | 3014027738 |
| Address | 6/8 rue Jean Antoine de Baif |
| City | PARIS CEDEX 13 Ile-de-France |
| Country | FR |
| Registration valid through | 2026 |
| Product codes listed | GXY |
| Device classes | 2 |
At a glance
- 1–9 Device listings
- 1–9 UDI devices (GUDID)
- Current Registration current
- None FDA inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device establishment registrations
Device establishments that manufacture, repackage, relabel or import devices for the U.S. market must register annually with the FDA and list the devices they produce.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database