Acotec Scientific Co., Ltd.
Active in EUDAMEDChinafrom SRN EUDAMED FDA SRN CN-MF-000015843 FEI 3015471899
- Devices
- 898
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
What Acotec Scientific Co., Ltd. makes
Acotec Scientific Co., Ltd. manufactures endovenous radiofrequency ablation devices, including the Cedar™ Endovenous Radiofrequency Catheter (ERA-C70-US and ERA-C30-US) and the Endovenous Radiofrequency Generator (ERA-G5-US). These products are designed for the treatment of venous insufficiency by thermally ablating varicose veins through controlled radiofrequency energy delivery.
The company’s portfolio is regulated under Class II medical devices in the US and includes products listed via the FDA’s 510(k) premarket notification process. The devices are intended for use in vascular procedures and are subject to compliance with FDA requirements for radiofrequency ablation systems.
Catalogue
Search and filter all 898 devicesShowing 201-250 of 898
Company details
- EUDAMED SRN
- CN-MF-000015843
- FDA FEI number
- 3015471899
- DUNS number
- 548757551
- EUDAMED status
- Active
- EUDAMED registered name
- Acotec Scientific Co., Ltd
- Registered address
- Courtyard No. 10, Longqing Street, 100176, Beijing, China
- Website
- www.acotec.cn/?lang=en
- [email protected]
- Phone
- +86 010 67872107
- PRRC contact
- Maddy Li