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Vaprox

by STERIS Corporation United States EUDAMED

Ref PB007Model VAPROX HC Sterilant

EMDN S900101

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number0724995MMVAPROXHCSTRL6L Basic UDI-DIDate13 Aug 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 24 Oct 2026

Device Name
VAPROX HC Sterilant
Model / Reference
VAPROX HC Sterilant, PB007
Primary DI / UDI-DI
00724995225551
Basic UDI-DI
0724995MMVAPROXHCSTRL6L
EMDN Code
S900101 Hydrogen peroxide cartridges
Device Class
Class IIa
Market of Registration
Ireland

Manufacturer details

EUDAMED SRN
US-MF-000016007
Authorised representative
STERIS Ireland Ltd IE-AR-000010065

Other devices from Steris Corporation

See all devices from Steris Corporation →

Properties & raw data

Show properties, registry sources and raw records
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

Sources (1)

  • EUDAMED 00724995225551|0724995MMVAPROXHCSTRL6L 61 fields · synced 24 Oct 2026