HomeChinaKonica Minolta Medical & Graphic (Shanghai) Co., Ltd.

Konica Minolta Medical & Graphic (Shanghai) Co., Ltd.

China · www.konicaminolta.com.cn
✓ Record-verifiedregistrations found in 11 marketsEU SRN JP-MF-000008214Unified social credit code 91310115739777475E

This company has registrations in European Union, United States, United Kingdom, Brazil, Saudi Arabia, Canada, Taiwan, Singapore, South Korea, Australia, Hong Kong — 11 overseas markets. No China NMPA registrations were found.

Registrations by market

Each market counts a different unit; figures are not directly comparable
CNChinaNMPA
0China registrations
as of 2026-09-01
EUEuropean UnionEUDAMED
265UDI-DI device records
Class I 138Class IIa 124Class IIb 3
USUnited StatesFDA openFDA
11listed device types
Class I 3Class II 8Class III 0
plus 153 registration records and 62 510(k)
UKUnited KingdomMHRA PARD
13registered device records
Class I 5Class IIa 8
BRBrazilANVISA
13registered devices
Class I 6Class II 7
22 including historic records
SASaudi ArabiaSFDA
4registered imported devices
low-risk imported devices only; a 2023 snapshot, not updated since
CACanadaMDALL
3active device licences
Class II 2Class III 1
25 including historic records
TWTaiwanTFDA
11valid device licences
Class I 1Class II 10
SGSingaporeHSA SMDR
8device registrations
CLASS B 8
KRSouth KoreaMFDS GMP
4GMP quality-system certificates
Import 4
AUAustraliaTGA ARTG
11active ARTG entries
Class I 1IIa 8IIb 2
HKHong KongMDACS
2valid listings
Class II 2
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.

European Union265 raw hits, 0 excluded, 265 confirmed
United States153 registration records, 62 510(k), 0 PMA
China0 certificates (Class III 0 / II 0 / I 0), as of 2026-09-01
United Kingdom13 confirmed, 0 excluded
Brazil13 confirmed, 0 excluded
Saudi Arabia4 confirmed, 0 excluded
Canada3 confirmed, 0 excluded
Manufacturer names merged into this page: KONICA MINOLTA TECHNOPRODUCTS CO., LTD. · Konica Minolta Healthcare Americas, Inc · KONICA MINOLTA, INC. · KONICA MINOLTA HEALTHCARE AMERICAS, INC. · KONICA MINOLTA HEALTHCARE DO BRASIL INDUSTRIA DE EQUIPAMENTOS MEDICOS LTDA · KONICA MINOLTA HEALTHCARE AMERICAS, INT

Regulatory identity

EU manufacturer SRN
JP-MF-000008214
EU authorised representative
Konica Minolta Business Solutions Europe GmbH
UK responsible person
KONICA MINOLTA Business Solutions (UK) Ltd.
Unified social credit code
91310115739777475E
Exhibition record
CMEF 89th (Apr 2024, Shanghai) · CMEF 87th (Spring 2023, Shanghai)

Company information

Country
China
Social-insurance enrolees
21
Annual revenue
over RMB 500M
Website
www.konicaminolta.com.cn

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
2002-06-10
Registered capital
USD 500,000
Paid-in capital
USD 500,000
Legal form
Limited liability company (wholly owned by a foreign corporation)
Industry classification
Wholesale trade
Last approval date
2026-01-07
Recognitions
Micro and small enterprise

Business registration data from Tianyancha, as of 2026-09-03. 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

22007
22008
12009
12010
32011
62012
12013
32014
32015
22016
22017
42018
12019
12020
42021
62022
12023
22024
12025
12026

FDA listed device types

showing 8 of 11
System, Image Processing, Radiological 1Transducer, Ultrasonic, Diagnostic 1Solid State X-Ray Imager (Flat Panel/Digital Imager) 1System, Imaging, Pulsed Echo, Ultrasonic 1Camera, Multi Format, Radiological 1System, Imaging, Pulsed Doppler, Ultrasonic 1Full Field Digital, System, X-Ray, Mammographic 1System, X-Ray, Stationary 1

Registration details (sample)

MarketIdentifierNameClass / date
EU04560141921238Class IIa
EU04560141922501Class IIa
EU04560141922372Class IIa
EU04560141920767Class IIa
UK17904DIRECT DIGITZERClass IIa
UK61109DIRECT DIGITIZERClass I
UK61109DIRECT DIGITIZERClass IIa
USK252996Universal 1417PI2026-06-12
USK250665SKR 30002025-06-17
USK241319SKR 30002024-11-21
BR80101380018RAD PACS - OPAL . EXAClass I
BR10303949037Medidor de icterícia JM-105Class II
BR80101389001FILMES PARA RAIOS XClass II
SAME0000009876SFDAA00005Medical Imaging Film SD-S
SAME0000009876SFDAA00003Drypro Laser Imager
CA66411REGIUS MODEL 370Class II
CA66414REGIUS MODEL 190Class III
CA88872AERODR STITCHING SYSTEMClass II

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