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Multichem CSF

by Techno-path Manufacturing Ltd.

Part of a family of 8 devices: see the family page

Ref 06S7802

Multichem CSF (06S7802) is a device classified as Class C in the EU and Class I in the US made by Techno-Path Manufacturing, registered in EUDAMED on 10 Aug 2026 (Basic UDI-DI 539152344CHEM075M) and listed in FDA GUDID since 2 Jun 2026 (UDI-DI 05391523442909), active as of 24 Oct 2026.

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

CE IVDR

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/IVDR EUDAMED Number539152344CHEM075M Basic UDI-DI 05391523442909UDI-DIDate10 Aug 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number05391523442909 UDI-DI Date2 Jun 2026ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 539152344CHEM075M registered 10 Aug 2026 Active
  • FDA GUDID UDI-DI 05391523442909 listed 2 Jun 2026 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 05391523442909
  2. Registered EUDAMED 539152344CHEM075M

Coverage

2 jurisdictions

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  • Withdrawn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

Specification

EUDAMED · GUDID

Generic name
Multiple-type clinical chemistry analyte profile IVD, control
Model / reference
06S7802
Primary DI / UDI-DI
05391523442909
Basic UDI-DI
539152344CHEM075M
FDA product code
JJY
EMDN code
W0101050208 Csf controls
GMDN term
Multiple-type clinical chemistry analyte profile IVD, control
Device class
Class C EUDAMED
Class I GUDID
Regulation number
862.1660
EU registration type
Standard device
EU market of registration
Ireland
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class C
GUDID
Class I

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

Manufacturer details

EUDAMED SRN
IE-MF-000001822

Similar devices in this category

Other devices filed under SPECIFIC CONTROLS (CLINICAL CHEMISTRY).

Other devices from Techno-Path Manufacturing

See all devices from Techno-Path Manufacturing →

Properties

  • Contains human tissues or cells
  • Professional testing
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (21, all answered No)