CHUNLI Spinal Fusion Device - Indonesia BPOM Medical Device Registration
CHUNLI Spinal Fusion Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21302320766. The device is manufactured by BEIJING CHUNLIZHENGDA MEDICAL INSTRUMENTS CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ASIA ACTUAL INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Country of Origin
China
Authorized Representative
PT. ASIA ACTUAL INDONESIAAR Address
PERKANTORAN GANDARIA 8 LANTAI 6 UNIT JL. SULTAN ISKANDAR MUDA KEBAYORAN LAMA UTARA JAKARTA SELATAN
Registration Date
Jul 11, 2023
Expiry Date
Mar 14, 2028
Product Type
Prosthetic Orthopedic Equipment
Intervertebral body fusion device
Non Electromedic Sterile
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