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isareverse™

by Move-Up 34 variants

Ref 0022I2615

isareverse™ (0022I2615) is a Class III device made by Move-Up, registered in EUDAMED on 12 Jun 2026 (Basic UDI-DI B-03701160201418), active as of 25 Oct 2026.

Active European Union

CE MDD

Valid until

No date given

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

Source EUDAMED, synced 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-03701160201418 Basic UDI-DI Date12 Jun 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device name
isareverse™Embase glénoïdienne Ø 26 mm sans ciment plot longueur 25 mm
isareverse™Embase glénoïdienne Ø 26 mm sans ciment plot longueur 15 mm
Model / reference
0022I2615
Primary DI / UDI-DI
03701160201418, 03701160201401
Basic UDI-DI
B-03701160201418, B-03701160201401
EMDN code
P09010301, P0901040199
Device class
Class III
EU registration type
Legacy device (under a directive)
EU market of registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000000412

Similar devices in this category

Other devices filed under EPIPHYSARY HUMERAL COMPONENTS - OTHER.

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Properties

  • Supplied sterile
  • Implantable
Other properties (10, all answered No)