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PathTezt® GS-2500

by Biocytech Corporation Sdn. Bhd.

Ref GS-2500Model 1. CS-36100 2. IS-36100 3. US-36100 4. HS-36100 5. CG-102450 6. GS-2500

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

CE IVDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

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

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR EUDAMED Number955102041SlideQL Basic UDI-DI 09551020410368UDI-DIDate29 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number09551020410368 UDI-DI Date11 Mar 2026ListedStatusListed GUDID: in commercial distribution

Certificates

0 certificates · EUDAMED

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

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  • Withdrawn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

Trade Name
PathTezt PreClean White Colour Glass Slide EUDAMED
PathTezt® GUDID
Generic Name
General specimen microscopy slide IVD, single-use
Device Name
PathTezt Consumable - Slide
Model / Reference
GS-2500, 1. CS-36100 2. IS-36100 3. US-36100 4. HS-36100 5. CG-102450 6. GS-2500
Primary DI / UDI-DI
09551020410368
Basic UDI-DI
955102041SlideQL
FDA Product Code
KEW
EMDN Code
W0503900201 Microscope slides
GMDN Term
General specimen microscopy slide IVD, single-use
Device Class
Class A EUDAMED
Class I GUDID
Regulation Number
864.3010
EU market of registration
Cyprus
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device ClassEUDAMED
Class A
GUDID
Class I

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Properties

  • Single Use
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (19)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Human Tissues: No
  • Animal Tissues: No
  • Microbial Substances: No
  • Reagent: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Professional Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No
  • New Device: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No