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H7F

by Graphite Medical EUDAMED

Active European Union

Ref H7F XL, H7F L, H7F S, H7F XXL, H7F XS

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number36156H7FFD Basic UDI-DIDate9 Mar 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED

Device Name
H7F
Model / Reference
H7F XL, H7F L, H7F S, H7F XXL, H7F XS
Primary DI / UDI-DI
03615650000576, 03615650000569, 03615650000545, 03615650000583, 03615650000538
Basic UDI-DI
36156H7FFD
EMDN Code
Y060624 Shoulder-elbow orthoses
Device Class
Class I
Market of Registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000002504

Other devices from Graphite Medical

See all devices from Graphite Medical →

Properties

Show 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