HomeGermanyGeister Medizin Technik GmbH

Geister Medizin Technik GmbH

Germany · Tuttlingen
✓ Record-verifiedregistrations found in 3 markets

This company has registrations in United States, Brazil, Canada — 3 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
49listed device types
Class I 39Class II 10Class III 0
plus 50 registration records and 6 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
30registered devices
Class I 28Class II 2
this export covers Class I / II only (the cadastro route)
SASaudi ArabiaSFDA
0registered imported devices
low-risk imported devices only; a 2023 snapshot, not updated since
CACanadaMDALL
4active device licences
Class II 4
TWTaiwanTFDA
pendingnot queried
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
pendingnot queried
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
pendingnot queried
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 States50 registration records, 6 510(k), 0 PMA
Brazil30 confirmed, 0 excluded
Canada4 confirmed, 0 excluded
Manufacturer names merged into this page: GEISTER MEDIZINTECHNIK GMBH · Geister medizintechnik Gmbh · Geister Mediszintechnik GmbH

Company information

Country
Germany
City
Tuttlingen

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 510(k) clearances by year

11994 · K933699
11999 · K982365
12003 · K030788
12004 · K022823
12018 · K180610
12025 · K242759

FDA listed device types

showing 8 of 49
Motor, Surgical Instrument, Ac-Powered 1Rasp 1Probe 1Sizer, Heart-Valve, Prosthesis 1Clamp 1Handle, Scalpel 1Saw, Electrically Powered 1Applier, Hemostatic Clip 1

Registration details (sample)

MarketIdentifierNameClass / date
USK242759Geister K-Rex rongeurs2025-06-06
USK180610Geister retractor for neuro - and spine surgery2018-08-29
USK022823VALVULOTOME, RETROGRADE : 03-7500- 03-7510, ANTEGRADE 03-75202004-07-01
BR81888830009Conjunto de Microinstrumentos, Tipo Rhoton, para Neurocirurgia em TitâClass I
BR81888830010Conjunto de Microinstrumentos, Tipo Rhoton, para Neurocirurgia em Aço Class I
BR80190320002KIT DE SEIS LÂMINAS ATRIAL COM SUPORTE E CLAMP INTRODUTORClass I
CA77443CONNECTOR/ADAPTOR (SUCTION TUBES, CANNULAS)Class II
CA77492SUCTION TUBE - STAINLESS STEELClass II
CA77665TITANIUM CLAMP/CLIPClass II

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