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Cellis

by Meccellis Biotech France EUDAMED

Ref CELLIS C2030EModel C55E

EMDN P900299

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number1434-MDR-012/2026 Date24 Apr 2026IssuedStatusActive expires 23 Apr 2031

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)

Specification

EUDAMED · synced 23 Oct 2026

Device Name
CELLIS 5 cm x 5 cm - 1.4 mm
Model / Reference
C55E, CELLIS C2030E
Primary DI / UDI-DI
03760256960042
Basic UDI-DI
3760256960CELLIS84
EMDN Code
P900299 Surgical meshes - other
Device Class
Class III
Market of Registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000002452

Other devices from Meccellis Biotech

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  • Cellis Breast

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See all devices from Meccellis Biotech →

Properties & raw data

Show properties, registry sources and raw records
  • Sterile
  • Implantable
  • Animal Tissues
Other properties (10)
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No

Sources (1)

  • EUDAMED 30048e5e-728a-44b7-8007-5e7d68a6b62d 61 fields · synced 23 Oct 2026