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Buffered saline solution 4ml

by VIAMAR INTERNATIONAL, s.r.o. Czech Republic EUDAMED

Ref 98350-200 EMDN W0104010206

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number85941999298237CA Basic UDI-DIDate9 Jan 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/IVDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 24 Oct 2026

Device Name
Pufrovaný fyziologický roztok
Model / Reference
98350-200
Primary DI / UDI-DI
08594199922301
Basic UDI-DI
85941999298237CA
EMDN Code
W0104010206 Media in tubes (solid & liquid)
Device Class
Class A
Market of Registration
Czechia

Manufacturer details

EUDAMED SRN
CZ-MF-000038013

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Properties & raw data

Show properties, registry sources and raw records
  • Reagent
  • Professional Testing
Other properties (9)
  • Sterile: No
  • Human Tissues: No
  • Animal Tissues: No
  • Microbial Substances: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No
  • New Device: No

Sources (1)

  • EUDAMED 4a4f6120-1061-4b53-9a24-b0e3193e19a0 61 fields · synced 24 Oct 2026