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Clean Protect

by sebia

Ref 2059

Clean Protect (2059) is a protein electrophoresis IVD (EU IVDR Class A; FDA Class I; FDA product code CEF, Electrophoretic, Protein Fractionation) made by Sebia, registered in EUDAMED on 18 Jul 2022 (Basic UDI-DI 3607362059BUCS) and listed in FDA GUDID since 16 Dec 2022 (UDI-DI 03607360020593), active as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing GUDID Number03607360020593 UDI-DI Date16 Dec 2022ListedStatusListed GUDID: in commercial distribution
European UnionCE/IVDR EUDAMED Number3607362059BUCS Basic UDI-DI 03607360020593UDI-DIDate18 Jul 2022RegisteredStatusActive

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 3607362059BUCS registered 18 Jul 2022 Active
  • FDA GUDID UDI-DI 03607360020593 listed 16 Dec 2022 Listed

Timeline

2 dated events

  1. Registered EUDAMED 3607362059BUCS
  2. Listed FDA GUDID 03607360020593

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  • Withdrawn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
Protein electrophoresis IVD, kit, electrophoresis
Model / Ref / Catalog
2059
Primary DI / UDI-DI
03607360020593
Basic UDI-DI
3607362059BUCS
FDA product code
CEF
EMDN code
W01019099 Clinical chemistry reagents - other
GMDN term
Protein electrophoresis IVD, kit, electrophoresis
Device class
Class A EUDAMED
Class I GUDID
Regulation number
862.1630
EU registration type
Standard device
EU market of registration
France
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class A
GUDID
Class I

Device class is stated on each registry's own scale: Class A 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
FR-MF-000003520

Related devices

Category: Nucleic acid extraction/isolation kit IVD

Similar devices in this category

Other devices filed under CLINICAL CHEMISTRY REAGENTS - OTHER.

Other devices from Sebia

See all devices from Sebia →

Properties

  • Reagent
  • IVD kit
  • Professional testing
  • Prescription use
  • Convenience kit
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (18, all answered No)