Sunrise - BEUDAMED

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1,681 results · 50ms · Sources: EU EUDAMED, US FDA

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FDA registration 824 Device 312 FDA UDI 232 FDA 510(k) 150 FDA Pre-Market Approval 69 Basic UDI-DI 64 Manufacturer 17 Authorized representative 10 Importer 3 + More Filters

Country

United States 772 Germany 256 China 185 United Kingdom 127 Taiwan 84 Australia 47 Mexico 25 Belgium 13 Netherlands 10 Finland 8 Vietnam 6 France 5 Spain 4 Austria 3 Argentina 1 Indonesia 1 Lithuania 1 Norway 1 Singapore 1 Switzerland 1 + More Countries

Manufacturer

Sunrise Medical Gmb H 155 Helping Hand Company (Ledbury) Ltd 126 Sunrise Medical (Us) Llc 49 Hubei Sunrise Protective Products Co., Ltd 14 Sunrise Sa 7 Red Milawa Pty Ltd T/A Magic Mobility 6 Sunrise Tech Enterprises Corp 6 Wenzhou Sunrise Industrial And Trading Co., Ltd 5 Hunan Sunrise Health Inc. 4 Shandong Zhushi Pharmaceutical Group Co., Ltd 4 Jiangsu Intco Medical Products Co., Ltd 3 Ankiya Bio Tec Co., Ltd. 2 Anhui Tiankang Medical Technology Co., Ltd. 2 Anhui Yodo Biotechnology Co.,Ltd 2 Anqing Kangmingna Packaging Co.,Ltd 2 Badiusen Biotechnology (Kunshan) Co., Ltd 2 Beijing Honghugaoxiang Science And Technology Development Co.,Ltd. 2 Beijing Nubway S&T Co., Ltd. 2 Beijing Zksk Technology Co., Ltd 2 Changsha Fourier Medical Technology Co.,Ltd. 2 + More Manufacturers

Competent Authority

De/Ca38 Regierungspräsidium Karlsruhe 218 Health Products Regulatory Authority, Medical Devices Department 127 Ministry Of Health, Welfare And Sports 19 Agencia Española De Medicamentos Y Productos Sanitarios 15 De/Ca20, Bezirksregierung Düsseldorf Dezernat 24 9 Federal Agency For Medicines And Health Products / / Health Products Division 8 De/Ca22 Bezirksregierung Münster 2 De/Ca30 Regierungspräsidium Kassel Dezernat 55 Medizinprodukte Und Produktsicherheitsrecht 2 De/Ca304 Marktüberwachung Medizinprodukte Bayern 2 The Medicines And Healthcare Products Regulatory Agency 2 Danish Medicines Agency, Pharmacovigilance & Medical Devices 1 The Norwegian Medical Products Agency 1 + More Competent Authorities

Kind

Single Use 15 Active 14 Measuring Function 1 Software 1 + More Kinds

Classification

Eu Md Class 1 374 FDA Class 2 118 FDA Class 3 66 FDA Class 1 32 FDA Unclassified 3 Eu Md Class 2a 2 + More Classifications

FDA FEI Number

3009171220 177 2011171 111 1721676 103 1820334 98 3002807314 98 3009380063 95 1000114185 65 1000116158 65 1000135961 65 1016427 65 1721686 65 2017233 65 3000206435 65 3001452571 65 3002534070 65 3002806434 65 3002808486 65 3003528016 65 3003565456 65 3003678543 65 + More FDA FEI Numbers

Regulation

Us FDA 1k Eu Mdr 376 + More Regulations

Authorized Representative

Sunrise Medical Gmb H 187 International Associates Auditing & Certification Limited 127 Sungo Europe B.V. 15 Riomavix Ltd 7 Humiss Beratung Gmb H 6 Joysun Group S.L.U 5 James Leckey Design Ltd 1 Kingsmead Service B.V. 1 Luxus Lebenswelt Gmb H 1 Med Net Ec Rep Gmb H 1 Med Path Gmb H 1 Rfx+Care International A/S 1 + More Authorized Representatives

FDA Registration Number

3009171220 177 2011171 111 1721676 103 1820334 98 3002807314 98 3009380063 95 1016427 65 1054811 65 1721686 65 2017233 65 2030624 65 2184009 65 2247858 65 2953200 65 3002808486 65 3003678543 65 3004497303 65 3005562917 65 3005580113 65 3006131984 65 + More FDA Registration Numbers

Status

On The Market 310 Not Intended For Eu Market 2 + More Statuses

MedPath GmbH

Authorized representative

🇩🇪 Germany·537 Manufacturers·13464 Devices

<1 …81 82 83 84 85 >

Data last updated 04 / 2026. Visit the official EUDAMED website for up-to-date data.

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EU MDR

EU MDR Medical Devices EU MDR Active Medical Devices EU MDR Class I Medical Devices EU MDR Class I Software Devices EU MDR Class IIa Medical Devices EU MDR Class IIa Software Devices EU MDR Class IIb Medical Devices EU MDR Class IIb Software Devices EU MDR Class III Medical Devices EU MDR Class III Software Devices EU MDR Implantable Medical Devices EU MDR Measuring Function Medical Devices EU MDR Software Medical Devices

EU IVDR

EU IVDR In Vitro Diagnostic Devices EU IVDR Class A In Vitro Diagnostic Devices EU IVDR Class A Software Devices EU IVDR Class B In Vitro Diagnostic Devices EU IVDR Class B Software Devices EU IVDR Class C In Vitro Diagnostic Devices EU IVDR Class C Software Devices EU IVDR Class D In Vitro Diagnostic Devices EU IVDR Class D Software Devices EU IVDR Instrument Devices EU IVDR Kit Devices EU IVDR Reagent Devices EU IVDR Software Devices

FDA

FDA Medical Devices FDA Class I Medical Devices FDA Class II Medical Devices FDA Class III Medical Devices

By Country

EU IVDR Medical Devices from China EU IVDR Medical Devices from France EU IVDR Medical Devices from Germany EU IVDR Medical Devices from Romania EU IVDR Medical Devices from United States EU MDR Medical Devices from China EU MDR Medical Devices from Egypt EU MDR Medical Devices from Finland EU MDR Medical Devices from France EU MDR Medical Devices from Germany EU MDR Medical Devices from Italy EU MDR Medical Devices from Pakistan EU MDR Medical Devices from Poland EU MDR Medical Devices from Spain EU MDR Medical Devices from Türkiye EU MDR Medical Devices from United Kingdom EU MDR Medical Devices from United States

Notified Bodies

BSI Group The Netherlands B.V. DEKRA Certification B.V. DNV Product Assurance AS POLSKIE CENTRUM BADAN I CERTYFIKACJI S.A. SGS Belgium NV TÜV Rheinland LGA Products GmbH TÜV SÜD Product Service GmbH UDEM Uluslararasi Belgelendirme Denetim Egitim Merkezi San. ve Tic. A.Ş.

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