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BEIJING RUICHENG MEDICAL SUPPLIES CO., LTD.

China · Beijing

✓ Record-verifiedregistrations found in 5 markets

This company has registrations in United States, Brazil, Taiwan, South Korea, Australia — 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

4listed device types

Class I 1Class II 3Class III 0

plus 3 registration records and 2 510(k)

UKUnited KingdomMHRA PARD

pendingnot queried

BRBrazilANVISA

18registered devices

Class I 5Class II 13

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

24valid device licences

Class I 24

SGSingaporeHSA SMDR

pendingnot queried

KRSouth KoreaMFDS GMP

6GMP quality-system certificates

Import 6

AUAustraliaTGA ARTG

5active ARTG entries

Class I 2IIa 2Class Is (sterile) 1

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 States3 registration records, 2 510(k), 0 PMA, 1 excluded

Brazil18 confirmed, 0 excluded

Manufacturer names merged into this page: BEIJING RUICHENG MEDICAL SUPPLIES CO., LTD. · BEIJIN RUICHENG MEDICAL SUPPLIED CO., LTD. · BEIJING RUICHENG MEDICAL SUPPLIES Co., LTD.

FDA 510(k) clearances by year

22022 · K222408

FDA listed device types

Gauze / Sponge,Nonresorbable For External Use 1Multiple Use Blood Lancet For Single Patient Use Only 1Single Use Only Blood Lancet Without An Integral Sharps Injury Prevention Feature 1Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature 1

Registration details (sample)

Market	Identifier	Name	Class / date
US	K222408	Disposable Safety Lancet	2022-11-29
US	K222034	RightLance Blood Lancing System	2022-09-07
BR	80102512213	LANCETAS MEDISIGN	Class II
BR	82533959041	Lanceta Estéril	Class II
BR	80560319033	Lanceta para Glicosímetro MedLevensohn	Class II

BEIJING RUICHENG MEDICAL SUPPLIES CO., LTD.

Registrations by market

How these numbers were verified

Company information

FDA 510(k) clearances by year

FDA listed device types

Registration details (sample)

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