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Microstream Advance MVINOH

by Oridion Medical 1987 Ltd.

Part of a family of 45 devices: see the family page

Ref MVINOH

Microstream Advance MVINOH is a device classified as Class IIa in the EU and Class II in the US made by Oridion Medical 1987 Ltd., registered in EUDAMED on 20 Aug 2026 (Basic UDI-DI 0763000B000003979) and listed in FDA GUDID since 23 Jul 2020 (UDI-DI 20884521761800), active as of 23 Oct 2026.

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number0763000B000003979 Basic UDI-DI 20884521761800UDI-DIDate20 Aug 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number20884521761800 UDI-DI Date23 Jul 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 0763000B000003979 registered 20 Aug 2026 Active
  • FDA GUDID UDI-DI 20884521761800 listed 23 Jul 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 20884521761800
  2. Registered EUDAMED 0763000B000003979

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
Microstream Advance
Generic name
Nasal oxygen cannula, carbon-dioxide-sampling
Device name
CO2 Sample Line, Non Intubated with O2
Model / reference
MVINOH
Primary DI / UDI-DI
20884521761800
Basic UDI-DI
0763000B000003979
FDA product code
CCK
EMDN code
R03010204 Oxygen administration tubings
GMDN term
Nasal oxygen cannula, carbon-dioxide-sampling
Device class
Class IIa EUDAMED
Class II GUDID
Regulation number
868.1400
EU registration type
Standard device
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution
MRI safety
MR Safe
Size
Length — 3 Meter

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class IIa
GUDID
Class II

Device class is stated on each registry's own scale: Class IIa in the EU (EUDAMED), Class II in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Nasal oxygen cannula, carbon-dioxide-sampling

Similar devices in this category

Other devices filed under OXYGEN ADMINISTRATION TUBINGS.

Other devices from Oridion Medical 1987 Ltd.

See all devices from Oridion Medical 1987 Ltd. →

Properties

  • Single use
  • Prescription use
  • Lot / batch number
  • Manufacturing date
Other properties (21, all answered No)