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Home›Switzerland›UNIMED S.A.

UNIMED S.A.

Switzerland · Lausanne
✓ Record-verifiedregistrations found in 4 markets

This company has registrations in United States, Brazil, Canada, Israel — 4 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
5listed device types
Class I 3Class II 2Class III 0
plus 5 registration records and 0 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
6registered devices
Class II 6
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
0active device licences
10 including historic records
TWTaiwanTFDA
0valid device licences
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
pendingnot queried
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
1registrations
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 States5 registration records, 0 510(k), 0 PMA, 5 excluded
Brazil6 confirmed, 4 excluded
Saudi Arabia0 confirmed, 4 excluded
Canada0 confirmed, 1 excluded
Manufacturer names merged into this page: UNIMED S.A. · UNIMED S/A

Company information

Country
Switzerland
City
Lausanne

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

Trocar 1Neurological Stereotaxic Instrument 1Needle, Gastro-Urology 1Tube, Ear Suction 1Needle, Biopsy, Cardiovascular 1

Registration details (sample)

MarketIdentifierNameClass / date
BR10287070041AGULHA REUTILIZÁVEL PARA BIÓPSIA DE TECIDO ÓSSEO E MEDULA ÓSSEA 2R2 - Class II
BR10287070042AGULHA REUTILIZÁVEL PARA OFTALMOLOGIA 2R2 - UNIMEDClass II
BR10287070043AGULHA REUTILIZÁVEL DE ANESTESIA E RADIOGRAFIA 2R2 - UNIMEDClass II

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