HomeChinaZHEJIANG YIGAO MEDICAL TECHNOLOGY CO., LTD.

ZHEJIANG YIGAO MEDICAL TECHNOLOGY CO., LTD.

China · Hangzhou
✓ Record-verifiedregistrations found in 6 markets

This company has registrations in United States, Brazil, Canada, Taiwan, Singapore, Australia — 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
7listed device types
Class I 3Class II 4Class III 0
plus 7 registration records and 1 510(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
2valid device licences
Class II 2
SGSingaporeHSA SMDR
1device registrations
CLASS B 1
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
12active ARTG entries
Class I 2IIa 9Class Is (sterile) 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 States7 registration records, 1 510(k), 0 PMA, 1 excluded
Brazil6 confirmed, 0 excluded
Manufacturer names merged into this page: ZHEJIANG YIGAO MEDICAL TECHNOLOGY CO., LTD.

Company information

Country
China
City
Hangzhou

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

12025 · K250132

FDA listed device types

Endoscopic Guidewire, Gastroenterology-Urology 1Dislodger, Stone, Basket, Ureteral, Metal 1Endoscopic Access Overtube, Gastroenterology-Urology 1Collector, Urine, (And Accessories) For Indwelling Catheter 1Medical Device Data System 1Accessories, Catheter 1Stapler, Skin 1

Registration details (sample)

MarketIdentifierNameClass / date
USK250132Ureteral Access Sheath2025-09-05
BR80518279017Sonda Extratora de Cálculo com PontaClass II
BR80518279010CANULA FLEXÍVEL DILATADORA E DE ASPIRAÇÃO ELEPHANTClass II
BR82195309018Cesta de extração de pedra urológica descartávelClass II

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