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Emdyca

Hematology / histology / cytology instrumentsHistology / cytologyVarious processing instruments for hystology / cytology

Automated coverslippers

EMDN code W0202059008

12 manufacturers, 18 models including 18 on the market, 5 countries

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Manufacturers registered in Europe (EUDAMED) 12
  • On the market
  • No longer marketed
  • 93/42 Former directive, not yet certified under the MDR
  • Click a manufacturer to see its full range, a model to open its EUDAMED record.
ManufacturerCountryRegistered modelsClassContact
Islandpolymer Germany A IVDR Website EUDAMED record Report an error
Leicabiosystems FDA Germany A IVDR Website support.de@LeicaBiosystems.com EUDAMED record Report an error
Sakura Seiki EU representative : Sakura Finetek Europe B.V. (Netherlands) Japan A IVDR Website EUDAMED record Report an error
Shandon Diagnostics FDA EU representative : Epredia Netherlands B.V. (Netherlands) United Kingdom (ex Northern Ireland) A IVDR EUDAMED record Report an error
Bio-Optica Milano FDA Italy A IVDR Website info@bio-optica.it EUDAMED record Report an error
Dakewe FDA EU representative : SUNGO Europe B.V. (Netherlands) China A IVDR Website EUDAMED record Report an error
Guangzhou Naturn Medical Devices EU representative : MedPath GmbH (Germany) China A IVDR EUDAMED record Report an error
Intelsint Italy A IVDR Website info@intelsint.com EUDAMED record Report an error
Jinquanmedical EU representative : SUNGO Europe B.V. (Netherlands) China A IVDR sales1@jinquanmedical.com EUDAMED record Report an error
Medite FDA Germany A IVDR Website EUDAMED record Report an error
Ningbo Chiwell Biotechnology FDA EU representative : SUNGO Europe B.V. (Netherlands) China A IVDR EUDAMED record Report an error
Slee FDA Germany A IVDR EUDAMED record Report an error

A model registered in EUDAMED is not necessarily sold in your country. Check availability and CE marking with the manufacturer.

Other manufacturers known in the United States (FDA) 9

Manufacturers selling this type of device in the United States according to the FDA, not yet in EUDAMED for this category. Some do sell in Europe: registration of devices already on the market is mandatory until 28 November 2026, and some are registered under their parent company’s name. The category is inferred automatically from the US classification and may include related products.

ManufacturerCountryBrandsFDA clearance
SAKURA FINETEK U.S.A., INC. Present in Europe in other categories United States Tissue-Tek Film® Tissue-Tek® Glas™ g2 Tissue-Tek® Glas™ Tissue-Tek® registered
Dakewe (Shenzhen) Medical Equipment Co., Ltd. China CS500 Glass Coverslipper registered
Epredia Holdings Ltd. United States – registered
IGE Medical Devices, LLC United States – registered
Leica Biosystems, division of Leica Microsystems, Inc. United States – registered
MEDIMEAS INSTRUMENTS India – registered
PT PHC Indonesia Indonesia – registered
Sakura Global Holding Company United States – registered
Sipcon Technologies Private Limited India – registered

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