Skip to content
Emdyca

Instruments for functional explorations and therapeutic interventionsNeurology and neurosurgery instrumentsInstruments for motorised neurosurgery systems

Drills for neurosurgery

EMDN code Z12100902

7 manufacturers, 61 models including 61 on the market, 6 countries

Export to CSV
Manufacturers registered in Europe (EUDAMED) 7
  • 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
Zethon FDA EU representative : De Soutter Medical Limited (Netherlands) United Kingdom (ex Northern Ireland)
33 others
I, IIa, III MDR, 93/42 regulatory@zethon.com EUDAMED record Report an error
Medtronic FDA EU representative : Medtronic B.V. (Netherlands) United States
11 others
IIa MDR EUDAMED record Report an error
Nefmed medikal ürünleri inşaat otomotiv dış ticaret A.Ş Türkiye IIa 93/42 Website info@nefmedical.com EUDAMED record Report an error
Aesculap FDA Germany IIa MDR Website eudamed@bbraun.com EUDAMED record Report an error
ClearPoint Neuro FDA EU representative : Emergo Europe B.V. (Netherlands) United States I MDR Website regulatory@clearpointneuro.com EUDAMED record Report an error
Micromar FDA EU representative : Emergo Europe B.V. (Netherlands) Brazil IIa MDR Website EUDAMED record Report an error
Nakanishi FDA EU representative : NSK Europe GmbH (Germany) Japan IIa 93/42 Website 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) 19

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
Acra Cut, Inc. United States Disposable Cranial Perforator ACRA-CUT Acra-Cut Reusable Cranial Perforator K032970 (2003)
evonos GmbH & Co. KG Germany Evonos K231403 (2024)
EMD Endoszkóp Műszer Gyártó és Kereskedelmi Korlátolt Felelősségű Társaság Present in Europe in other categories – NeuroLine registered
adeor Medical AG Germany Meridian Perforator registered
INTEGRA LIFESCIENCES PRODUCTION CORPORATION Present in Europe in other categories United States CODMAN® registered
STRYKER CORPORATION Present in Europe in other categories United States Zyphr registered
Synthes GmbH Present in Europe in other categories United States – registered
The Anspach Effort, Inc. United States – K082637 (2008)
AD Supply Group Limited United Kingdom – registered
CBR Enterprise Limited Hong Kong SAR China – registered
Emd Endoszkop Muszer Gyarto ES Kereskedelmi Kft. Hungary – K213228 (2022)
Guizhou Zirui Technology Co., Ltd. China – K254177 (2026)
Integra LifeSciences Corporation Present in Europe in other categories United States – K183581 (2019)
MILLSTONE MEDICAL OUTSOURCING LLC. United States – registered
Mainline Medical Dental Supply Canada – registered
SYNTHES GMBH / Synthes Produktions GmbH United States – registered
Sanicure BV Netherlands – registered
Unique Instruments Inc. United States – registered
Worldwide Supplies Limited Hong Kong SAR China – registered

Didn't find it?

Tell us what you are looking for. Requests show us which categories to add first.

Related categories