Shanghai Wonderful Opto-Electrics Tech.Co.,Ltd - BEUDAMED

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21 results · 229ms · Sources: EU EUDAMED, US FDA

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FDA registration 7 FDA 510(k) 6 FDA UDI 3 Authorized representative 1 Basic UDI-DI 1 Certificate 1 Device 1 Manufacturer 1 + More Filters

Country

China 17 United States 3 Germany 1 + More Countries

Manufacturer

Shanghai Wonderful Opto Electrics Tech.Co.,Ltd 4 Beatles Medical Supplies(xiantao)co., Ltd 1 Foshan United Medical Technologies Ltd 1 Henan Tuoren Xin Hui Medical Technology Co.,Ltd. 1 Shende (Ningbo) Medical Device Technology Co., Ltd 1 Weihai Kangzhou Biotechnology Engineering Co.,Ltd 1 Zhejiang Helowin Medical Technology Co., Ltd 1 Zhejiang Pushkang Biotechnology Co., Ltd. 1 + More Manufacturers

Competent Authority

De/Ca304 Marktüberwachung Medizinprodukte Bayern 5 + More Competent Authorities

Kind

Active 1 Reusable 1 + More Kinds

Classification

FDA Class 2 6 Eu Md Class 2b 2 + More Classifications

Notified Body

Notice Belgelendirme, Muayene Ve Denetim Hizmetleri Anonim şirketi 4 + More Notified Bodies

FDA FEI Number

3004505220 13 3001431138 6 1000120578 5 1000548922 5 1000597018 5 1419489 5 2027755 5 2916735 5 3005515469 5 3005581016 5 3005972890 5 3006515340 5 3007120647 5 3007712511 5 3008915316 5 3010175098 5 3011877721 5 3012294783 5 3015262665 5 3017125161 5 + More FDA FEI Numbers

Regulation

Us FDA 16 Eu Mdd 2 + More Regulations

Authorized Representative

Medwheat Tech Service Gmb H 4 + More Authorized Representatives

FDA Registration Number

3004505220 13 3001431138 6 1000548922 5 1222993 5 1419489 5 2027755 5 2916735 5 3005515469 5 3005581016 5 3005972890 5 3006515340 5 3007120647 5 3007712511 5 3008915316 5 3010175098 5 3011877721 5 3012294783 5 3015262665 5 3017125161 5 3017181358 5 + More FDA Registration Numbers

Certificate Type

Mdd Annex Ii (Excluding Section 4) 4 + More Certificate Types

Status

On The Market 1 + More Statuses

Diosculpt

FDA Class 2 ·General, Plastic Surgery

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

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EU MDR

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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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