CURAWAY Semi-Automatic Core Biopsy Instruments - Indonesia BPOM Medical Device Registration
CURAWAY Semi-Automatic Core Biopsy Instruments is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10801420441. The device is manufactured by ZHEJIANG CURAWAY MEDICAL TECHNOLOGY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. PURE SOUTHEAST ASIA INDONESIA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
ZHEJIANG CURAWAY MEDICAL TECHNOLOGY CO., LTD.Country of Origin
China
Authorized Representative
PT. PURE SOUTHEAST ASIA INDONESIAAR Address
Equity Tower, 26th Floor H, Kav 52-53, Jl. Jenderal Sudirman
Registration Date
Dec 22, 2024
Expiry Date
Jun 25, 2029
Product Type
Diagnostic Gastroenterology-Urology Equipment
Gastroenterology-urology biopsy instrument (biopsy forceps cover and non-electric biopsy forceps)
Non Electromedic Sterile
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