HomeChinaBEIJING HANBAIHAN MEDICAL DEVICES CO., LTD.

BEIJING HANBAIHAN MEDICAL DEVICES CO., LTD.

China · Beijing
✓ Record-verifiedregistrations found in 6 markets

This company has registrations in United States, Brazil, Canada, Australia, Hong Kong, Israel — 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
pendingnot queried
EUEuropean UnionEUDAMED
pendingnot queried
USUnited StatesFDA openFDA
4listed device types
Class I 2Class II 2Class III 0
plus 5 registration records and 0 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
13registered devices
Class II 13
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
6 including historic records
TWTaiwanTFDA
pendingnot queried
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
7active ARTG entries
IIa 7
HKHong KongMDACS
1valid listings
Class II 1
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 States5 registration records, 0 510(k), 0 PMA
Brazil13 confirmed, 0 excluded
Manufacturer names merged into this page: BEIJING HANBAIHAN MEDICAL DEVICES CO., LTD. · BEIJING HANBAIHAN MEDICAL DEVICES CO., LTD

Company information

Country
China
City
Beijing

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

Platelet And Plasma Separator For Bone Graft Handling 1Laser, Comb, Hair 1System, Blood Collection, Vacuum-Assisted, Manual 1Centrifuges (Micro, Ultra, Refrigerated) For Clinical Use 1

Registration details (sample)

MarketIdentifierNameClass / date
BR82495259012Conjunto para Tratamento da Dor Crônica LEVmaxClass II
BR82495259013RegenHairClass II
BR82495259019VEROClass II

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