HomeChinaAMSINO MEDICAL (SHANGHAI) CO., LTD.

AMSINO MEDICAL (SHANGHAI) CO., LTD.

China · Shanghai
✓ Record-verifiedregistrations found in 2 markets

This company has registrations in United States, Taiwan — 2 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
22listed device types
Class I 6Class II 16Class III 0
plus 29 registration records and 1 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
0registered devices
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
1valid device licences
Class I 1
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
pendingnot queried
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 States29 registration records, 1 510(k), 0 PMA, 6 excluded
Brazil0 confirmed, 3 excluded
Saudi Arabia0 confirmed, 2 excluded
Canada0 confirmed, 1 excluded
Manufacturer names merged into this page: AMSINO MEDICAL INC. · AMSINO MEDICAL (SHANGHAI) CO., LTD.

Company information

Country
China
City
Shanghai

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

12021 · K201138

FDA listed device types

showing 8 of 22
Filter, Bacterial, Breathing-Circuit 1Tracheostomy Cleaning Tray 1Uroflowmeter 1Catheter And Tip, Suction 1Catheter, Ureteral, Gastro-Urology 1Tube, Aspirating, Flexible, Connecting 1Bottle, Collection, Vacuum 1Apparatus, Suction, Operating-Room, Wall Vacuum Powered 1

Registration details (sample)

MarketIdentifierNameClass / date
USK201138AMSure® Single Use Saline Topical Solution2021-04-14

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