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Motiva Implants

by Establishment Labs EUDAMED

Active European Union

Ref RVF-235+Model Motiva Implants Round VelvetSurface Plus

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR NumberMDR 798371 Date12 Jun 2026IssuedStatusActive expires 1 Jan 2030

Coverage

1 jurisdiction

NorwayNorwayIcelandNorwaySwedenFinlandFinlandNorwaySwedenFinlandFinlandNorwaySwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceLiechtensteinAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalyTürkiyeTürkiyeSpainSpainCroatiaGreeceTürkiyeTürkiyeTürkiyeTürkiyeMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

EU market availability

Made available in 32 countries, as listed in EUDAMED:

Declared by the manufacturer in EUDAMED for this device version; may not cover every market.

  • Austria since 2 Jan 2025
  • Belgium since 2 Jan 2025
  • Bulgaria since 2 Jan 2025
  • Croatia since 2 Jan 2025
  • Cyprus since 2 Jan 2025
  • Czechia since 2 Jan 2025
  • Denmark since 2 Jan 2025
  • Estonia since 2 Jan 2025
  • Finland since 2 Jan 2025
  • France since 2 Jan 2025
  • Germany since 2 Jan 2025
  • Greece since 2 Jan 2025
  • Hungary since 2 Jan 2025
  • Iceland since 2 Jan 2025
  • Ireland since 2 Jan 2025
  • Italy since 2 Jan 2025
  • Latvia since 2 Jan 2025
  • Liechtenstein since 2 Jan 2025
  • Lithuania since 2 Jan 2025
  • Luxembourg since 2 Jan 2025
  • Malta since 2 Jan 2025
  • Netherlands since 2 Jan 2025
  • Northern Ireland since 2 Jan 2025
  • Norway since 2 Jan 2025
  • Poland since 2 Jan 2025
  • Portugal since 2 Jan 2025
  • Romania since 2 Jan 2025
  • Slovakia since 2 Jan 2025
  • Slovenia since 2 Jan 2025
  • Spain since 2 Jan 2025
  • Sweden since 2 Jan 2025
  • Türkiye since 2 Jan 2025

Last checked 24 Oct 2026.

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • MDR 798371 Supplemented

    Technical documentation EU MDR

    Notified body
    Notified body 2797
    Issued
    12 Jun 2026
    Expires
    1 Jan 2030
    Reason
    Change approved

Specification

EUDAMED

Model / Reference
Motiva Implants Round VelvetSurface Plus, RVF-235+
Primary DI / UDI-DI
07445161005243
Basic UDI-DI
7445161VelvetPlus62
EMDN Code
P0601010202,X020102
Device Class
Class III
Market of Registration
Belgium

Manufacturer details

EUDAMED SRN
CR-MF-000008155
Authorised representative
Emergo Europe B.V. NL-AR-000000116

Other devices from Establishment Labs

See all devices from Establishment Labs →

Properties

  • Sterile
  • Implantable

Other properties (11)

  • 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