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Resvent Medical Technology Co., Ltd

China · Shenzhen Guangdong · www.resvent.com

✓ Record-verifiedregistrations found in 10 marketsEU SRN CN-MF-000012608Unified social credit code 91440300358733444J

This company holds 13 NMPA certificates in China and has registrations in European Union, United States, Brazil, Canada, Singapore, Australia, Hong Kong, Israel, Russia — 9 overseas markets.

Registrations by market

Each market counts a different unit; figures are not directly comparable

CNChinaNMPA

13China registrations

Class II 11Class III 2

as of 2026-09-04

EUEuropean UnionEUDAMED

35UDI-DI device records

Class IIa 30Class IIb 5

USUnited StatesFDA openFDA

6listed device types

Class I 3Class II 1Class III 0unclassified 2

plus 6 registration records and 1 510(k)

UKUnited KingdomMHRA PARD

0registered device records

BRBrazilANVISA

5registered devices

Class II 5

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

8 including historic records

TWTaiwanTFDA

pendingnot queried

SGSingaporeHSA SMDR

2device registrations

CLASS B 2

KRSouth KoreaMFDS GMP

pendingnot queried

AUAustraliaTGA ARTG

1active ARTG entries

IIa 1

HKHong KongMDACS

3valid listings

Class II 3

ILIsraelAMAR

3registrations

RURussiaRoszdravnadzor

1active registrations

Class 2b 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 Union35 raw hits, 0 excluded, 35 confirmed

United States6 registration records, 1 510(k), 0 PMA

China13 certificates (Class III 2 / II 11 / I 0), as of 2026-09-04

Brazil5 confirmed, 0 excluded

Manufacturer names merged into this page: RESVENT MEDICAL TECHNOLOGY CO., LTD.

Regulatory identity

EU manufacturer SRN: CN-MF-000012608
EU authorised representative: Eunitor GmbH
Unified social credit code: 91440300358733444J
Exhibition record: CMEF 87th (Spring 2023, Shanghai) · CMEF 89th (Apr 2024, Shanghai) · CMEF 93rd (Apr 2026, Shanghai)

Business registration

Registration status: Active
Incorporated: 2015-10-13
Registered capital: CNY 2,521,102
Paid-in capital: CNY 2,409,014
Legal form: Limited liability company
Industry classification: Wholesale trade
Last approval date: 2025-12-25
Recognitions: Micro and small enterpriseNational High-Tech EnterpriseTechnology-based SMESRDI SME

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

12026 · K253044

FDA listed device types

Ventilator, Non-Continuous (Respirator) 1Continuous Ventilator, Minimal Ventilatory Support 1Non-Continuous Ventilator For Emergency Use 1Support, Breathing Tube 1Medical Device Data System 1Circuit, Breathing (W Connector, Adaptor, Y Piece) 1

Registration details (sample)

Market	Identifier	Name	Class / date
CN	国械注准20243080599	呼吸机	Class III
CN	国械注准20223080484	呼吸机	Class III
CN	粤械注准20262080937	加温呼吸管路	Class II
CN	粤械注准20262080934	呼吸管路	Class II
EU	06970819423267	Nasal Mask	Class IIa
EU	06970819423274	Nasal Mask	Class IIa
EU	06970819421706	Nasal Mask	Class IIa
EU	06970819422215	Nasal Mask	Class IIa
US	K253044	RXiBreeze PAP System (RXiBreeze 20C)	2026-07-23
BR	80117589144	Full Face Mask	Class II
BR	80117589146	Nasal Mask	Class II
BR	80117589147	Tube	Class II