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INFUSION CUFF 3000 ml with manometer, bladder and air release valve

by Friedrich Bosch GmbH&Co.KG EUDAMED

Active European Union

Ref 5001.11.020Model F BOSCH INFUSION CUFF

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number4260157895001.0193 Basic UDI-DIDate3 May 2025RegisteredStatusActive

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  • Withdrawn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
Infusion Cuff
Model / Reference
F BOSCH INFUSION CUFF, 5001.11.020
Primary DI / UDI-DI
04260157892316
Basic UDI-DI
4260157895001.0193
Direct Marketing DI
04260157892316
EMDN Code
Z12030399 Infusion instruments - other
Device Class
Class I
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000005955

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Properties

Show properties
  • Contains Latex
  • Measuring Function
Other properties (11)
  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Incorporates Medicinal Product: No