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Reliance

by STERIS Canada ULC 16 variants

Ref FH420009Model Reliance PTX Endoscope Processing System

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number0724995QBRELPTXEPSBU Basic UDI-DI 00724995155841UDI-DIDate25 Jun 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Reliance PTX Endoscope Processing System
Model / Reference
Reliance PTX Endoscope Processing System, FH420009
Primary DI / UDI-DI
00724995155841
Basic UDI-DI
0724995QBRELPTXEPSBU
EMDN Code
Z12011301 Cleaning and disinfection equipment
Device Class
Class IIb
Market of Registration
Ireland

Manufacturer details

EUDAMED SRN
CA-MF-000017563
Authorised representative
STERIS Ireland Ltd IE-AR-000010065

Other devices from STERIS Canada ULC

See all devices from STERIS Canada ULC →

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