HomeChinaHEBEI DINGLI MEDICAL APPARATUS AND INSTRUMENT CO., LTD

HEBEI DINGLI MEDICAL APPARATUS AND INSTRUMENT CO., LTD

China · Hengshui City Hebei
✓ Record-verifiedregistrations found in 3 markets

This company has registrations in United States, Saudi Arabia, Russia — 3 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
10listed device types
Class I 9Class II 1Class III 0
plus 10 registration records and 0 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
0registered devices
this export covers Class I / II only (the cadastro route)
SASaudi ArabiaSFDA
1registered 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
pendingnot queried
ILIsraelAMAR
pendingnot queried
RURussiaRoszdravnadzor
1active registrations
Class 1 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 States10 registration records, 0 510(k), 0 PMA, 1 excluded
Saudi Arabia1 confirmed, 0 excluded
Manufacturer names merged into this page: HEBEI DINGLI MEDICAL APPARATUS AND INSTRUMENT CO., LTD · HEBEI DINGLI MEDICAL APPARATUS AND INDUSTRUMENT CO.,LTD

Company information

Country
China
City
Hengshui City Hebei

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 listed device types

showing 8 of 10
Cushion, Flotation 1Orthosis, Truncal/Orthosis, Limb 1Cabinet, Table And Tray, Anesthesia 1Cart, Emergency, Cardiopulmonary (Excluding Equipment) 1Sling, Arm 1Bag, Reservoir 1Orthosis, Cervical 1Bed, Manual 1

Registration details (sample)

MarketIdentifierNameClass / date
SAME0000015499SFDAA00001DINGLI

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