HomeGermanyNEUROMEDEX GmbH.

NEUROMEDEX GmbH.

Germany · Hamburg Schleswig-Holstein
✓ Record-verifiedregistrations found in 5 markets

This company has registrations in United States, Brazil, Australia, Hong Kong, Israel — 5 overseas markets. The China NMPA lookup is still pending.

Registrations by market

Each market counts a different unit; figures are not directly comparable
CNChinaNMPA
n/aThis registry lists domestic registrants only
EUEuropean UnionEUDAMED
pendingnot queried
USUnited StatesFDA openFDA
1listed device types
Class I 0Class II 1Class III 0
plus 2 registration records and 0 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
2registered devices
Class II 2
3 including historic records
SASaudi ArabiaSFDA
0registered imported devices
low-risk imported devices only; a 2023 snapshot, not updated since
CACanadaMDALL
0active device licences
TWTaiwanTFDA
pendingnot queried
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
7active ARTG entries
Class I 1Class III 1IIa 1Class Is (sterile) 4
HKHong KongMDACS
2valid listings
Class II 1Class IV 1
ILIsraelAMAR
3registrations
RURussiaRoszdravnadzor
pendingnot queried
Not yet connected: India CDSCO, Indonesia Kemenkes. The public search for Japan PMDA and Vietnam IMDA does not return manufacturer names, so entries cannot be linked to companies coming — where there is no data it is shown as "pending", never estimated.

How these numbers were verified

record-verified

Company-name search in every official database is a substring match and returns same-named but different companies. Each figure below is the count after re-checking every record against the manufacturer name.

United States2 registration records, 0 510(k), 0 PMA
Brazil2 confirmed, 0 excluded
Manufacturer names merged into this page: Neuromedex GmbH · NEUROMEDEX GMBH · NEUROMEDEX GmbH.

Company information

Country
Germany
City
Hamburg Schleswig-Holstein

Fields marked "pending" have not been obtained yet; that does not mean they do not exist. Risk records (litigation, penalties, operating anomalies) are kept internal and not published.

FDA listed device types

Neurological Stereotaxic Instrument 1

Registration details (sample)

MarketIdentifierNameClass / date
BR80088060011ELETRODOS DE USO ÚNICO PARA RADIOFREQUÊNCIAClass II
BR81044960001Cânula Descartável para RadiofrequênciaClass II

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