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Tube 48010

by Chromsystems Instruments & Chemicals GmbH

Ref 48010

Tube 48010 is a general laboratory container (EU IVDD general IVD; FDA Class I; FDA product code LXG) made by Chromsystems Instruments & Chemicals GmbH, registered in EUDAMED on 21 Sep 2026 (Basic UDI-DI B-04250317510174) and listed in FDA GUDID since 31 Jul 2025 (UDI-DI 04250317510174), 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-04250317510174 Basic UDI-DI 04250317510174UDI-DIDate21 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04250317510174 UDI-DI Date31 Jul 2025ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-04250317510174 registered 21 Sep 2026 Active
  • FDA GUDID UDI-DI 04250317510174 listed 31 Jul 2025 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04250317510174
  2. Registered EUDAMED B-04250317510174

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  • Withdrawn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
Glass Tubes for hydrolysis EUDAMED
Tube GUDID
Generic name
General laboratory container, single-use
Model / Ref / Catalog
48010
Primary DI / UDI-DI
04250317510174
Basic UDI-DI
B-04250317510174
FDA product code
LXG
EMDN code
W01019099 Clinical chemistry reagents - other
GMDN term
General laboratory container, single-use
Device class
Class IVD General EUDAMED
Class I GUDID
Regulation number
862.2050
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: General laboratory container, single-use

Similar devices in this category

Other devices filed under CLINICAL CHEMISTRY REAGENTS - OTHER.

Other devices from Chromsystems Instruments & Chemicals GmbH

See all devices from Chromsystems Instruments & Chemicals GmbH →

Properties

  • Reagent
  • Professional testing
  • Premarket exempt
  • Expiration date
  • Manufacturing date
Other properties (21, all answered No)