HomeGermanyTHUASNE DEUTSCHLAND GMBH

THUASNE DEUTSCHLAND GMBH

Germany · Burgwedel Lower Saxony
✓ Record-verifiedregistrations found in 5 markets

This company has registrations in United States, Saudi Arabia, Taiwan, Australia, 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
12listed device types
Class I 12Class II 0Class III 0
plus 12 registration records and 0 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
0registered devices
this export covers Class I / II only (the cadastro route)
SASaudi ArabiaSFDA
21registered imported devices
low-risk imported devices only; a 2023 snapshot, not updated since
CACanadaMDALL
0active device licences
TWTaiwanTFDA
4valid device licences
Class I 4
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
2active ARTG entries
Class I 2
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
2registrations
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 States12 registration records, 0 510(k), 0 PMA, 3 excluded
Saudi Arabia21 confirmed, 3 excluded
Manufacturer names merged into this page: THUASNE DEUTSCHLAND GMBH · THUASNE Deutschland GmbH

Company information

Country
Germany
City
Burgwedel Lower Saxony

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

showing 8 of 12
Prosthesis, Breast, External, Used With Adhesive 1Orthosis, Limb Brace 1Joint, Knee, External Brace 1Orthosis, Lumbar 1Prosthesis, Breast, External, No Adhesive 1Orthosis, Abdominal 1Component, External, Limb, Ankle/Foot 1Support, Arm 1

Registration details (sample)

MarketIdentifierNameClass / date
SAME0000000683SFDAA00006SILIMA Classic
SAME0000000683SFDAA00013Rhizo PRO

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