Skip to content

Pufferolt fiziológiás sóoldat Plus 3000 ml

by REAGENS Fejlesztő, Gyártó és Kereskedelmi Kft.

Ref 15020Model Pufferolt fiziológiás sóoldat Plus

Active European Union

CE IVDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

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/IVDR Number599654715PBSPLUSE4 Basic UDI-DI 05996547150207UDI-DIDate25 May 2022RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/IVDR Active

Specification

EUDAMED

Device Name
Pufferolt fiziológiás sóoldat Plus
Model / Reference
Pufferolt fiziológiás sóoldat Plus, 15020
Primary DI / UDI-DI
05996547150207
Basic UDI-DI
599654715PBSPLUSE4
EMDN Code
W0101070304 Common buffers and solutions (electrolytes)
Device Class
Class A
EU market of registration
Hungary

Manufacturer details

EUDAMED SRN
HU-MF-000019161

Other devices from REAGENS Fejlesztő, Gyártó és Kereskedelmi Kft.

See all devices from REAGENS Fejlesztő, Gyártó és Kereskedelmi Kft. →

Properties

  • Reagent

Other properties (10)

  • Sterile: No
  • Human Tissues: No
  • Animal Tissues: No
  • Microbial Substances: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Professional Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No
  • New Device: No