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Remeex Readjustment Kit

by Desarrollo E Investigacion Medica Aragonesa S.L. 2 variants

Ref AR-01LP

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number843656835REMEEXREADJUSTEE Basic UDI-DI 08437007606096UDI-DIDate18 Sep 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Remeex Readjustment Kit
Model / Reference
AR-01LP
Primary DI / UDI-DI
08437007606096
Basic UDI-DI
843656835REMEEXREADJUSTEE
EMDN Code
U1299 Single-use urogenital instrumentation (non-endoscopic) - other
Device Class
Class IIa
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
ES-MF-000004008

Other devices from Desarrollo E Investigacion Medica Aragonesa SL

See all devices from Desarrollo E Investigacion Medica Aragonesa SL →

Properties

  • Sterile

Other properties (12)

  • 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