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Rea Clematis Pro

by Invacare France Operations SAS 21 variants

Ref DV1685766 and suffix, DV1673805 and suffix, DV1685771 and suffix, DV1682347 and suffix, DV1682350 and suffix, DV1682352 and suffix, DV1661455 and suffix, DV1682342 and suffix, DV1673545 and suffix, DV1676332 and suffix, DV1685768 and suffix, DV1673812 and suffix, DV1676334 and suffix, DV1676338 and suffix, DV1661457 and suffix, DV1676333 and suffix, DV1682351 and suffix, DV1676335 and suffix, DV1676340 and suffix, DV1676331 and suffix, DV1661456 and suffix, DV1685767 and suffix, DV1682344 and suffix, DV1661458 and suffix, DV1682349 and suffix, DV1682370 and suffix, DV1673813 and suffix, DV1673806 and suffix, DV1661459 and suffix, DV1676339 and suffix

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, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number3662050ClematisProLP Basic UDI-DI Date19 Nov 2025RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference
DV1685766 and suffix, DV1673805 and suffix, DV1685771 and suffix, DV1682347 and suffix, DV1682350 and suffix, DV1682352 and suffix, DV1661455 and suffix, DV1682342 and suffix, DV1673545 and suffix, DV1676332 and suffix, DV1685768 and suffix, DV1673812 and suffix, DV1676334 and suffix, DV1676338 and suffix, DV1661457 and suffix, DV1676333 and suffix, DV1682351 and suffix, DV1676335 and suffix, DV1676340 and suffix, DV1676331 and suffix, DV1661456 and suffix, DV1685767 and suffix, DV1682344 and suffix, DV1661458 and suffix, DV1682349 and suffix, DV1682370 and suffix, DV1673813 and suffix, DV1673806 and suffix, DV1661459 and suffix, DV1676339 and suffix
Primary DI / UDI-DI
03662050469045, 03662050275363, 03662050469090, 03662050464002, 03662050464033, 03662050464057, 03662050173294, 03662050463951, 03662050275349, 03662050276674, 03662050469069, 03662050275400, 03662050276698, 03662050276735, 03662050173317, 03662050276681, 03662050464040, 03662050276704, 03662050276759, 03662050276667, 03662050173300, 03662050469052, 03662050463975, 03662050173324, 03662050464026, 03662050464231, 03662050275417, 03662050275370, 03662050173331, 03662050276742
Basic UDI-DI
3662050ClematisProLP
EMDN Code
Y122106, Y122103
Device Class
Class I
EU market of registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000006807

Other devices from Invacare France Operations SAS

See all devices from Invacare France Operations SAS →

Properties

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