CURAWAY Endovenous Radiofrequency Catheter - Indonesia BPOM Medical Device Registration
CURAWAY Endovenous Radiofrequency Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603421000. The device is manufactured by ZHEJIANG CURAWAY MEDICAL TECHNOLOGY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PURE SOUTHEAST ASIA INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ZHEJIANG CURAWAY MEDICAL TECHNOLOGY CO., LTD.Country of Origin
China
Authorized Representative
PURE SOUTHEAST ASIA INDONESIAAR Address
Equity Tower, 26th Floor H, Kav 52-53, Jl. Jenderal Sudirman
Registration Date
May 09, 2024
Expiry Date
Jan 10, 2029
Product Type
Surgical Equipment
Electrosurgical cutting and coagulation device and accessories.
Non Radiation Electromedics
CURAWAY Disposable Biopsy Needle
CURAWAY Semi-Automatic Core Biopsy Instruments
CURAWAY Automatic Core Biopsy Instruments
CURAWAY Radiofrequency Generator
CURAWAY Cura RF Electrode
CURAWAY Endovenous Radiofrequency Generator
CuraFlex Pressure Bandage
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