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Precolumn Cartridge 18032

by Chromsystems Instruments & Chemicals GmbH

Ref 18032

Precolumn Cartridge 18032 is an in vitro diagnostic device (EU IVDD general IVD; FDA Class I; FDA product code KZR, Chromatography (Liquid, Gel), Clinical Use; EMDN category clinical chemistry reagents) made by Chromsystems Instruments & Chemicals GmbH, registered in EUDAMED on 17 Sep 2026 (Basic UDI-DI B-04250317519863) and listed in FDA GUDID since 27 Aug 2020 (UDI-DI 04250317519863), active as of 24 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 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDD EUDAMED NumberB-04250317519863 Basic UDI-DI 04250317519863UDI-DIDate17 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04250317519863 UDI-DI Date27 Aug 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-04250317519863 registered 17 Sep 2026 Active
  • FDA GUDID UDI-DI 04250317519863 listed 27 Aug 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04250317519863
  2. Registered EUDAMED B-04250317519863

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  • Withdrawn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
Precolumn cartridge 4/10 EUDAMED
Precolumn Cartridge GUDID
Generic name
High performance liquid chromatography analyser column IVD
Model / Ref / Catalog
18032
Primary DI / UDI-DI
04250317519863
Basic UDI-DI
B-04250317519863
FDA product code
KZR
EMDN code
W01019099 Clinical chemistry reagents - other
GMDN term
High performance liquid chromatography analyser column IVD
Device class
Class IVD General EUDAMED
Class I GUDID
Regulation number
862.2260
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: High performance liquid chromatography analyser column IVD

Similar devices in this category

Other devices filed under CLINICAL CHEMISTRY REAGENTS - OTHER.

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Properties

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