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Slide Laser Printer

by Guangzhou Labsim Biotech Co., Ltd

Ref REF-TESTModel G364P, G306U, G364D, G306I, G264D, G264P, G363UV

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number697013603040DZ Basic UDI-DI Date6 Aug 2026RegisteredStatusActive

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  • Withdrawn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

Model / Reference
G364P, REF-TEST, G306U, G364D, G306I, G264D, G264P, G363UV
Primary DI / UDI-DI
06970136030407, 06970136030759, 06970136030360, 06970136030766, 06970136030780, 06970136030773, 06970136030087
Basic UDI-DI
697013603040DZ, 697013603075EL, 69701360303603Q, 697013603076EN, 697013603078ES, 697013603077EQ, 697013603008E5
Direct Marketing DI
06970136030407
06970136030759
06970136030360
06970136030766
06970136030780
06970136030773
06970136030087
EMDN Code
W0299 IVD instruments - other
Device Class
Class A
EU market of registration
Germany
Spain

Manufacturer details

EUDAMED SRN
CN-MF-000002446
Authorised representative
CMC Medical Devices & Drugs SL ES-AR-000000293

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Properties

  • Professional Testing
  • Surgical Instrument
  • New Device NoEUDAMEDYesEUDAMED

Other properties (8)

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