HomeChinaNANTONG MEDICAL

NANTONG MEDICAL

China · 南通 · www.chinajianghai.com
✓ Record-verifiedregistrations found in 9 marketsEU SRN CN-MF-000030315Unified social credit code 91320612138726154J

This company holds 39 NMPA certificates in China and has registrations in European Union, United States, United Kingdom, Brazil, Saudi Arabia, Australia, Israel, Russia — 8 overseas markets. EU UDI-DI records ≥234, the first 300 verified individually.

Registrations by market

Each market counts a different unit; figures are not directly comparable
CNChinaNMPA
39China registrations
Class I 19Class II 12
as of 2026-09-04
EUEuropean UnionEUDAMED
≥234UDI-DI device records
Class I 209IVD A 25
large result set — only the first 300 records were verified, so the real figure is at least this
USUnited StatesFDA openFDA
58listed device types
Class I 53Class II 5Class III 0
plus 66 registration records and 3 510(k)
UKUnited KingdomMHRA PARD
7registered device records
Class I 7
BRBrazilANVISA
5registered devices
Class I 5
this export covers Class I / II only (the cadastro route)
SASaudi ArabiaSFDA
2registered 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
19active ARTG entries
Class I 17IIa 2
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
11registrations
RURussiaRoszdravnadzor
1active registrations
Class 3 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.

European Union1,705 raw hits, 66 excluded, 234 confirmed. Large result set — only the first 300 verified
United States66 registration records, 3 510(k), 0 PMA, 23 excluded
China39 certificates (Class III 0 / II 12 / I 19), as of 2026-09-04
United Kingdom7 confirmed, 7 excluded
Brazil5 confirmed, 7 excluded
Saudi Arabia2 confirmed, 3 excluded
Canada0 confirmed, 2 excluded
Manufacturer names merged into this page: NANTONG CITY YOJO MEDICAL PRODUCTS CO., LTD. · NANTONG KANGJINCHEN MEDICAL EQUIPMENT CO., LTD. · NANTONG JIANAN MEDICAL PRODUCTS CO.,LTD · Tops Medical Articles Industries Nantong Inc · NANTONG STRIP MEDICAL SUPLY CO. LTD. · NANTONG JIANAN MEDICAL PRODUCTS CO., LTD

Regulatory identity

EU manufacturer SRN
CN-MF-000030315
EU authorised representative
SUNGO Europe B.V.
UK responsible person
Partners for Endoscopy Limited
Unified social credit code
91320612138726154J
Exhibition record
CMEF 93rd (Apr 2026, Shanghai) · CMEF 89th (Apr 2024, Shanghai) · CMEF 87th (Spring 2023, Shanghai)

Company information

Country
China
Social-insurance enrolees
64
Annual revenue
RMB 50–100M
Website
www.chinajianghai.com
Product categories
手术器械

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.

Business registration

Registration status
Active
Incorporated
1979-11-26
Registered capital
CNY 58,180,000
Paid-in capital
CNY 10,180,000
Legal form
Limited liability company (foreign-invested, not wholly owned)
Industry classification
Special-purpose equipment manufacturing
Last approval date
2026-03-24
Recognitions
Micro and small enterpriseNational High-Tech Enterprise

Business registration data from Tianyancha, as of 2026-09-02. Public registry information only; legal representative and contact-person details are not collected. The figure is the number of employees enrolled in social insurance as declared by the company, which may differ from actual headcount.

FDA 510(k) clearances by year

12017 · K173043
22021 · K212264

FDA listed device types

showing 8 of 58
Cap, Surgical 1Pad, Eye 1Cushion, Flotation 1Forceps 1Mouthpiece, Breathing 1Scissors, Medical, Disposable 1Orthosis, Lumbar 1Mask, Oxygen, Non-Rebreathing 1

Registration details (sample)

MarketIdentifierNameClass / date
CN苏械注准20262030828一次性使用硬导丝Class II · 2026-06-15
CN苏械注准20182061034电动摄影平床Class II
CN苏械注准20172150241电动手术台Class II
CN苏械注准20162150855眼科手术台Class II
EU16958888002405Class I
EU06958888002422Class I
EU06958888004006Class I
EU06980367930001Class I
UK62145Disposable Air Water and suction valveClass I
UK64367Disposable Tray LinerClass I
UK47606Nasal stripsClass I
USK212264Surgical Face mask2021-11-13
USK203426Surgical Face Mask (non-sterile)2021-02-18
USK173043Holycon Synthetic Absorbable Sutures2017-12-14
BR10369469024Lenço para Assepsia em Procedimentos MédicosClass I
BR10369460033ALCOHOL PRE PADClass I
BR82799190002Máscara cirúrgica tripla descartávelClass I
SAME0000001511SFDAA00003gauze sponges
SAME0000001511SFDAA00004Gauze roll

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