Identity
- Trade Name
- Obesimed Forte CE sachet 21 st EUDAMED
- Device Name
- Obesimed Forte EUDAMED
- Model / Reference
- 042664 EUDAMED
Identifiers
- Primary DI / UDI-DI
- D-042664N9 EUDAMED
- Basic UDI-DI
- B-042664N9 EUDAMED
- EMDN Code
- G0402 ORALLY ADMINISTERED DEVICES FOR APPETITE CONTROL AND REDUCTION OF INTESTINAL ABSORPTION EUDAMED
Classification
- Device Class
- Class IIa EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Implantable
No
EUDAMED
Reusable
No
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Obesimed Forte CE sachet 21 st by PK Benelux BV — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDD
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-042664N9 | Class IIa | Active |
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Manufacturer
- Manufacturer
- PK Benelux BV
- EUDAMED SRN
- NL-MF-000006672
Sources (1)
- EUDAMED ab338f39-6eb6-4e39-aadb-760ce6a40db7 61 fields · synced Jul 22, 2026