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Obesimed Max Forte

EUDAMED

Class IIa (EU MDR)

Ref 953530Ref 073606

by PK Benelux BV

Identity

Trade Name
Obesimed Max Forte EUDAMED
Device Name
Carb & Fatblocker EUDAMED
Model / Reference
953530 EUDAMED
073606 EUDAMED

Identifiers

Primary DI / UDI-DI
D-953530RS EUDAMED
D-073606P3 EUDAMED
Basic UDI-DI
B-953530RS EUDAMED
B-073606P3 EUDAMED
EMDN Code
G0402 ORALLY ADMINISTERED DEVICES FOR APPETITE CONTROL AND REDUCTION OF INTESTINAL ABSORPTION EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany EUDAMED
Slovenia 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 Max Forte 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

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Manufacturer

Manufacturer
PK Benelux BV
EUDAMED SRN
NL-MF-000006672

Sources (2)

  • EUDAMED 59478876-a4f4-47c2-868f-317eed23d63a 61 fields · synced Aug 4, 2026
  • EUDAMED 18715798-7951-43e7-9c2d-ceafdf7de1e0 61 fields · synced May 18, 2026