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Aps-19

by Matsunami Glass Ind., Ltd. 5 variants

Ref APS-39, SUAPS39Model APS Adhesive Glass Slide, IHC Adhesive Glass Slide

Active European Union

CE IVDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number49462474APS19PC Basic UDI-DI 04946247475637UDI-DIDate27 Nov 2023RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/IVDR Active

Specification

EUDAMED

Trade Name
APS Adhesive Glass Slide
Device Name
Aps-19
Microscope Slide
Model / Reference
APS Adhesive Glass Slide, APS-39, IHC Adhesive Glass Slide, SUAPS39
Primary DI / UDI-DI
04946247475637
Basic UDI-DI
49462474APS19PC, 494624742IHC0GB
EMDN Code
W0503900201 Microscope slides
Device Class
Class A
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
JP-MF-000023949
Authorised representative
Medical Technology Promedt Consulting GmbH DE-AR-000000085

Other devices from Matsunami Glass Ind., Ltd.

See all devices from Matsunami Glass Ind., Ltd. →

Properties

  • Professional Testing NoEUDAMEDYesEUDAMED

Other properties (10)

  • Sterile: No
  • Human Tissues: No
  • Animal Tissues: No
  • Microbial Substances: No
  • Reagent: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No
  • New Device: No