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Plasma Control Bi-Level 0071

by Chromsystems Instruments & Chemicals GmbH

Ref 0071

Plasma Control Bi-Level 0071 is a device classified as IVD General (EU), Class I (US) made by Chromsystems Instruments & Chemicals GmbH, registered in EUDAMED on 18 Sep 2026 (Basic UDI-DI B-04250317514974) and listed in FDA GUDID since 30 Jul 2020 (UDI-DI 04250317514974), active as of 23 Oct 2026.

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

CE IVDD

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/IVDD EUDAMED NumberB-04250317514974 Basic UDI-DI 04250317514974UDI-DIDate18 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04250317514974 UDI-DI Date30 Jul 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-04250317514974 registered 18 Sep 2026 Active
  • FDA GUDID UDI-DI 04250317514974 listed 30 Jul 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04250317514974
  2. Registered EUDAMED B-04250317514974

Coverage

2 jurisdictions

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  • Withdrawn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

Specification

EUDAMED · GUDID

Trade name
Plasma Control Bi-Level (I+II) EUDAMED
Plasma Control Bi-Level GUDID
Generic name
Homocysteine IVD, control
Model / Ref / Catalog
0071
Primary DI / UDI-DI
04250317514974
Basic UDI-DI
B-04250317514974
FDA product code
JJX
EMDN code
W0101050299 Specific controls (cc) - other
GMDN term
Homocysteine IVD, control
Device class
Class IVD General EUDAMED
Class I GUDID
Regulation number
862.1660
EU registration type
Legacy device (under a directive)
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class IVD General
GUDID
Class I

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

Related devices

Category: Homocysteine IVD, control

Similar devices in this category

Other devices filed under SPECIFIC CONTROLS (CC) - OTHER.

Other devices from Chromsystems Instruments & Chemicals GmbH

See all devices from Chromsystems Instruments & Chemicals GmbH →

Properties

  • Reagent
  • Professional testing
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (21, all answered No)