HomeChinaSuzhou Zhenwu Medical Co., Ltd.

Suzhou Zhenwu Medical Co., Ltd.

China · Suzhou Jiangsu
✓ Record-verifiedregistrations found in 5 markets

This company has registrations in United States, Brazil, Hong Kong, Israel, Russia — 5 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
1listed device types
Class I 0Class II 1Class III 0
plus 2 registration records and 1 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
2registered devices
Class II 2
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
pendingnot queried
HKHong KongMDACS
1valid listings
Class II 1
ILIsraelAMAR
1registrations
RURussiaRoszdravnadzor
1active registrations
Class 2a 1
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 States2 registration records, 1 510(k), 0 PMA
Brazil2 confirmed, 0 excluded
Manufacturer names merged into this page: Suzhou Zhenwu Medical Co., Ltd. · SUZHOU ZHENWU MEDICAL CO., LTD

Company information

Country
China
City
Suzhou Jiangsu

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

12023 · K223208

FDA listed device types

Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature 1

Registration details (sample)

MarketIdentifierNameClass / date
USK223208Safety Lancet2023-02-10
BR10150470532Lancetas de segurança WiltexClass II
BR80686369016Sterile lancetClass II

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