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Emdyca

Instruments for functional explorations and therapeutic interventionsNeurology and neurosurgery instrumentsVarious neurology and neurosurgery instruments

Various neurology and neurosurgery instruments - other

EMDN code Z12109099

15 manufacturers, 150 models including 150 on the market, 10 countries

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Manufacturers registered in Europe (EUDAMED) 15
  • 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
Mizuho FDA EU representative : Emergo Europe B.V. (Netherlands) Japan
120 others
III MDR, 93/42 regulatory@mizuho.co.jp EUDAMED record Report an error
Invamed FDA Türkiye III 93/42 Website EUDAMED record Report an error
E.M.S Italy I, III MDR Website sales@emsmedical.net EUDAMED record Report an error
Eemagine FDA Germany IIa MDR Website EUDAMED record Report an error
Elekta FDA Sweden I MDR EUDAMED record Report an error
Meika Group Italy I, IIa MDR EUDAMED record Report an error
NICO FDA EU representative : Atlantico Systems, Ltd. (Ireland) United States IIa, III MDR Website info@NICOneuro.com EUDAMED record Report an error
SYNDEO Medical FDA Belgium IIa, IIb MDR EUDAMED record Report an error
Abbott FDA EU representative : Abbott Medical (Belgium) United States IIb MDR EUDAMED record Report an error
Balt Usa FDA EU representative : BALT EXTRUSION SAS (France) United States IIa 93/42 Website PRRC@baltgroup.com EUDAMED record Report an error
EB Neuro FDA Italy IIb MDR Website info@ebneuro.com EUDAMED record Report an error
Evasc EU representative : Emergo Europe B.V. (Netherlands) Canada III MDR Website EUDAMED record Report an error
IGEA FDA Italy IIa MDR Website EUDAMED record Report an error
Marginum Finland IIb MDR Website EUDAMED record Report an error
Shenzhen Med-link Electronics Tech FDA EU representative : Shanghai International Holding Corp. GmbH(Europe) (Germany) China IIa 93/42 Website sales@med-linket.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) 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
Peter Lazic GmbH Germany LAZIC K180757 (2019)
Aesculap, Inc. Present in Europe in other categories United States AESCULAP K131500 (2014)
Medicon eG. Chirurgiemechaniker-Genossenschaft – Medicon registered
NOVO SURGICAL, INC. – Novo Surgical Novosurgical Novo Surgical Inc. registered
ASPEN SURGICAL PRODUCTS, INC. Present in Europe in other categories United States – registered
Medicon EG Germany – K010908 (2001)
Rudolf Medical GmbH + Co. KG Germany – registered
STERIPAC GMBH Germany – registered
TELEFLEX INCORPORATED Present in Europe in other categories United States – registered

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