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Ossview

by CurveBeam LLC

Ref 1.8Model 1.X

Ossview (1.8) is a Class IIa device made by CurveBeam LLC, registered in EUDAMED on 9 May 2026 (Basic UDI-DI 8600045500441.XAE), active as of 22 Oct 2026.

Active European Union

CE MDR

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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8600045500441.XAE Basic UDI-DI 00860004550044UDI-DIDate9 May 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / reference
1.X, 1.8
Primary DI / UDI-DI
00860004550044
Basic UDI-DI
8600045500441.XAE
Direct marketing DI
00860004550044
EMDN code
V92 Medical device software - not included in other classes
Device class
Class IIa
Special device type
Software
EU registration type
Standard device
EU market of registration
France

Manufacturer details

EUDAMED SRN
US-MF-000004033
Authorised representative
ea-services FR-AR-000003449

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Properties

  • Measuring function
Other properties (13, all answered No)