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Bima

by B.I.M.A. Plastteknik Ab EUDAMED

Active European Union

Ref 10-3535-PModel 10-Series and C10-Series, 73400473(C)10-SERIESTR

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR NumberB-07340047300811 Basic UDI-DIDate17 Dec 2025RegisteredStatusActive
European UnionCE/MDD NumberB-07340047300811 Basic UDI-DIDate17 Dec 2025RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR, CE/MDD Active

Certificates: none listed in EUDAMED

Specification

EUDAMED

Device Name
Bima basic recond and Bima basic recond child
Model / Reference
10-Series and C10-Series, 10-3535-P, 73400473(C)10-SERIESTR
Primary DI / UDI-DI
07340047300811
Basic UDI-DI
B-07340047300811, 73400473(C)10-SERIESTR
Direct Marketing DI
07340047300811
EMDN Code
V080399 Medical cushions - other
Device Class
Class I
Market of Registration
Sweden

Manufacturer details

EUDAMED SRN
SE-MF-000001678

Other devices from B.I.M.A. Plastteknik Ab

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    Class I

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    Class I

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  • Bima

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See all devices from B.I.M.A. Plastteknik Ab →

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