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Refrigel

by Securimed France EUDAMED

Ref 1373, 0392 EMDN M9001

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number37011402pochesdegelDV Basic UDI-DIDate22 May 2023RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 22 Oct 2026

Device Name
Refrigel
Model / Reference
1373, 0392
Primary DI / UDI-DI
03701140200134, 03701140200882
Basic UDI-DI
37011402pochesdegelDV
EMDN Code
M9001 Cryotherapy and thermotherapy devices
Device Class
Class I
Market of Registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000006782

Other devices from Securimed

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Properties & raw data

Show properties, registry sources and raw records
Other properties (13)
  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No

Sources (2)

  • EUDAMED 310a0f3b-fcfa-437f-9f64-166c68a7e1d9 61 fields · synced 22 Oct 2026
  • EUDAMED 03701140200882|37011402POCHESDEGELDV 61 fields · synced 18 May 2026