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GENOUROB

France FR-MF-000029224 Last updated 23 Oct 2026

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Devices
4
Registries
EUDAMEDFDA
FDA recalls
0

Catalogue4

  • Rotab Ref ROTAB

    Class IIa EUDAMED Active
  • Dyneelax Ref Dyneelax

    Class IIa EUDAMED Active
  • Gnrb Ref GNRB

    Class IIa EUDAMED Active
  • Rotam Ref ROTAM

    Class IIa EUDAMED Active

Information

Country
France
Address
Bâtiment 60, Rue Henri Géret, Laval, France
Website
genourob.com
Phone
+33 243904301
PRRC contact
Nadège Macke
EUDAMED SRN
FR-MF-000029224
FDA FEI number
3008191251