HomeChinaBEIJING HANGTIAN KADI TECHNOLOGY R&D INSTITUTE

BEIJING HANGTIAN KADI TECHNOLOGY R&D INSTITUTE

China · Beijing
✓ Record-verifiedregistrations found in 3 markets

This company has registrations in United States, Brazil, Australia — 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
pendingnot queried
EUEuropean UnionEUDAMED
pendingnot queried
USUnited StatesFDA openFDA
5listed device types
Class I 2Class II 3Class III 0
plus 5 registration records and 2 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
4registered devices
Class II 4
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
TWTaiwanTFDA
pendingnot queried
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
1active ARTG entries
IIa 1
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 States5 registration records, 2 510(k), 0 PMA
Brazil4 confirmed, 0 excluded
Manufacturer names merged into this page: BEIJING HANGTIAN KADI TECHNOLOGY R&D INSTITUTE

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 510(k) clearances by year

22018 · K172846

FDA listed device types

Stabilizer, Heart 1Holder, Heart-Valve, Prosthesis 1Cannula, Manipulator/Injector, Uterine 1Laparoscope, General & Plastic Surgery 1Lavage, Jet 1

Registration details (sample)

MarketIdentifierNameClass / date
USK172846Uterine Manipulator2018-06-26
USK172789Specimen Retrieval Bag2018-02-01
BR82330859002Manipulador Uterino/injetor Oltramed - Ângulo Ajustável IClass II
BR82330859003Manipulador Uterino/injetor Oltramed - Ângulo Ajustável IIClass II
BR82330859004Manipulador Uterino/injetor Oltramed - Ângulo Fixo IClass II

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