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SFP230 - EndoStream Pure - non-sterile

by Partners for Endoscopy Limited EUDAMED

Withdrawn No longer placed on the EU market

Ref SFP230Model EndoStream

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-05060498721110 Basic UDI-DIDate30 Apr 2026RegisteredStatusWithdrawn No longer placed on the EU market

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Withdrawn

Certificates: none listed in EUDAMED

Specification

EUDAMED

Device Name
SFP230 - EndoStream Pure - non-sterile
Model / Reference
EndoStream, SFP230
Primary DI / UDI-DI
05060498721110
Basic UDI-DI
B-05060498721110
EMDN Code
Z12020585,Z12020685
Device Class
Class IIa

Manufacturer details

EUDAMED SRN
GB-MF-000021668
Authorised representative
Advena Limited MT-AR-000000234

Other devices from Partners for Endoscopy Limited

See all devices from Partners for Endoscopy Limited →

Properties

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