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Sanyrene

EUDAMED

Class IIa (EU MDR)

Ref 754304Ref 754237Ref 754240Ref 754239

by Laboratoires Urgo

Identity

Trade Name
SANYRENE EUDAMED
Device Name
SANYRENE - CORPITOL EUDAMED
Model / Reference
754304 EUDAMED
754237 EUDAMED
754240 EUDAMED
754239 EUDAMED

Identifiers

Primary DI / UDI-DI
03546890041336 EUDAMED
03546890040544 EUDAMED
03546890040575 EUDAMED
03546890040568 EUDAMED
Basic UDI-DI
354689UM00104K EUDAMED
EMDN Code
M9002 PROTECTIVE DEVICES, LUBRICANTS AND SOOTHING DEVICES (SPRAYS, GELS, FLUIDS AND CREAMS) EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Sanyrene by Laboratoires Urgo — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Laboratoires Urgo
EUDAMED SRN
FR-MF-000002559

Sources (4)

  • EUDAMED 4ba56499-d146-429e-941d-af8348b24778 61 fields · synced Aug 4, 2026
  • EUDAMED 422ded12-e127-48fd-aa31-4f7da256b82d 61 fields · synced May 17, 2026
  • EUDAMED c2e7bb0b-4ec8-4012-b33f-fbba7a857a9a 61 fields · synced May 17, 2026
  • EUDAMED 5891f817-f94d-4d56-a2e2-ca243e5d2858 61 fields · synced May 19, 2026