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Emdyca

Instruments for functional explorations and therapeutic interventionsOrthopaedic instrumentsVarious orthopaedic and traumatology instruments

Plaster cast saws

EMDN code Z12139005

26 manufacturers, 34 models including 34 on the market, 6 countries

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Manufacturers registered in Europe (EUDAMED) 26
  • 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
Vehu Germany I MDR Website info@vehu.com EUDAMED record Report an error
INVIDIA Medical Germany I MDR info@invidia-medical.de EUDAMED record Report an error
Mehrish EU representative : ANTEX MEDI SOLUTION (Germany) Pakistan I MDR Website EUDAMED record Report an error
Micromed FDA Germany I MDR Website info@micromed.com EUDAMED record Report an error
Surtex Instruments FDA EU representative : CMC Medical Devices & Drugs SL (Spain) United Kingdom (ex Northern Ireland) I MDR Website info@surtex-instruments.co.uk EUDAMED record Report an error
Weldoninstrument FDA EU representative : CMC Medical Devices & Drugs SL (Spain) Pakistan I 93/42 Website EUDAMED record Report an error
Zepf Medical Instruments Germany I MDR Website info@zepf-medical-instruments.de EUDAMED record Report an error
Amnotec Germany I MDR Website EUDAMED record Report an error
AR Instrumed EU representative : AR Instrumed Deutschland GmbH (Germany) Pakistan I MDR Website info@ar-instrumed.com EUDAMED record Report an error
BSN Medical FDA EU representative : BSN medical GmbH (Germany) United States I MDR EUDAMED_LAA1_LM_Charlotte@essity.com EUDAMED record Report an error
Centralsurgical FDA EU representative : KHANG BAO INTERNATIONAL KFT (Hungary) Pakistan I MDR Website EUDAMED record Report an error
ELCON Medical Instruments Germany I MDR Website info@elcon-medical.de EUDAMED record Report an error
Eltek Instruments FDA EU representative : CS Active (Latvia) Pakistan I MDR info@eltekinstruments.com EUDAMED record Report an error
Hilbro International FDA EU representative : CMC Medical Devices & Drugs SL (Spain) Pakistan I MDR sales.hilbrointl@gmail.com EUDAMED record Report an error
Medezine EU representative : European Healthcare & Device Solutions Ltd. (Ireland) United Kingdom (ex Northern Ireland) I MDR Website sales@medezine.co.uk EUDAMED record Report an error
Medicure EU representative : Yellow's medical instruments GmbH (Germany) Pakistan I MDR Website info@medicure.pk EUDAMED record Report an error
Medizintechnik FDA Germany I MDR Website info@AS-Medizintechnik.de EUDAMED record Report an error
Nadeemsurgical EU representative : KHANG BAO INTERNATIONAL KFT (Hungary) Pakistan I MDR Website info@nadeemsurgical.com EUDAMED record Report an error
Nopa FDA Germany I MDR Website info@nopa.de EUDAMED record Report an error
Oscimedsa FDA EU representative : OSCIMED EUROPE SAS (France) Switzerland I MDR Website info@oscimedsa.com EUDAMED record Report an error
Raydentinst EU representative : ANTEX MEDI SOLUTION (Germany) Pakistan I 93/42 Website info@raydentinst.com EUDAMED record Report an error
Rebstock FDA Germany I MDR Website info@rebstock.de EUDAMED record Report an error
REDA Instrumente FDA Germany I MDR Website EUDAMED record Report an error
Ruijinmedical FDA EU representative : CMC Medical Devices & Drugs SL (Spain) China I MDR Website info@whruijin.com EUDAMED record Report an error
Sheffmed FDA EU representative : Advena Limited (Malta) United Kingdom (ex Northern Ireland) I MDR Website EUDAMED record Report an error
Zethon FDA EU representative : De Soutter Medical Limited (Netherlands) United Kingdom (ex Northern Ireland) I MDR regulatory@zethon.com 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) 26

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
DE SOUTTER MEDICAL LIMITED United Kingdom De Soutter Medical registered
STRYKER CORPORATION Present in Europe in other categories United States – registered
Aesculap, Inc. Present in Europe in other categories United States – registered
Auxein Medical Pvt Ltd India – registered
BAERAMED INSTRUMENTE Germany – registered
Brasseler U.S.A. Medical, LLC Present in Europe in other categories United States – registered
CM INSTRUMENTE GMBH Germany – registered
DIMEDA INSTRUMENTE GMBH Germany – registered
Disruptive MedTech, LLC United States – registered
ENDONEST MEDICAL SYSTEMS LLP India – registered
GEISTER MEDIZINTECHN Germany – registered
GENTELL United States – registered
Good Medica sp.zo.o. Poland – registered
HEBUMEDICAL GMBH Germany – registered
Hangzhou Zhengda Medical CO.,LTD Present in Europe in other categories China – registered
JIANGSU SENOLO MEDICAL TECHNOLOGY CO., LTD. China – registered
MED2B LTD. Germany – registered
MEDLINE INDUSTRIES, INC. Present in Europe in other categories United States – registered
Manman Manufacturing Company Private Limited India – registered
NARANG MEDICAL, LTD. Present in Europe in other categories India – registered
Prime Medical LLC Present in Europe in other categories South Korea – registered
Sanicure BV Netherlands – registered
Sterramed Inc United States – registered
Techtronic Industries Medical Inc United States – registered
ZEPF MEDICAL INSTRUM Germany – registered
ZHEJIANG LONGYOU LANDMEDICAL TECHNOLOGY CO.,LTD. China – registered

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