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gbo Medizintechnik AG

Germany · Rimbach · www.gbo-med.de

✓ Record-verifiedregistrations found in 6 markets

This company has registrations in United States, United Kingdom, Canada, Taiwan, Hong Kong, Russia — 6 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

0UDI-DI device records

USUnited StatesFDA openFDA

4listed device types

Class I 1Class II 3Class III 0

plus 3 registration records and 0 510(k)

UKUnited KingdomMHRA PARD

1registered device records

Class IIa 1

BRBrazilANVISA

0registered devices

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

9active device licences

Class II 9

TWTaiwanTFDA

2valid device licences

Class II 2

SGSingaporeHSA SMDR

pendingnot queried

KRSouth KoreaMFDS GMP

pendingnot queried

AUAustraliaTGA ARTG

pendingnot queried

HKHong KongMDACS

2valid listings

Class II 2

ILIsraelAMAR

pendingnot queried

RURussiaRoszdravnadzor

3active registrations

Class 2a 3

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.

European Union9,598 raw hits, 100 excluded, 0 confirmed. Large result set — only the first 300 verified

United States3 registration records, 0 510(k), 0 PMA

United Kingdom1 confirmed, 53 excluded

Canada9 confirmed, 0 excluded

Manufacturer names merged into this page: GBO MEDIZINTECHNIK AG

Regulatory identity

UK responsible person: MDSS-UK RP LIMITED

Market	Identifier	Name	Class / date
UK	46573	me2.vie	Class IIa
CA	893	NEOSERV 824	Class II
CA	894	NEURO STIMULATORS	Class II
CA	898	SONOSTAT 833	Class II

gbo Medizintechnik AG

Registrations by market

How these numbers were verified

Regulatory identity

Company information

FDA listed device types

Registration details (sample)

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