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SFP160 - ScopeFlow Pure for Pentax 'scopes

by Partners for Endoscopy Limited EUDAMED

Active European Union

Ref SFP160Model ScopeFlow

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-05060498721035 Basic UDI-DIDate30 Apr 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Expiring

Certificates: none listed in EUDAMED

Specification

EUDAMED

Device Name
SFP160 - ScopeFlow Pure for Pentax 'scopes
Model / Reference
ScopeFlow, SFP160
Primary DI / UDI-DI
05060498721035
Basic UDI-DI
B-05060498721035
EMDN Code
Z12020585,Z12020685
Device Class
Class IIa
Market of Registration
Austria

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
  • Sterile
Other properties (10)
  • 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