SANYOU Spinal Fusion Cage Instrument - Indonesia BPOM Medical Device Registration
SANYOU Spinal Fusion Cage Instrument is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11303520028. The device is manufactured by SHANGHAI SANYOU MEDICAL CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is TRANSMEDIC INDONESIA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
SHANGHAI SANYOU MEDICAL CO., LTD.Country of Origin
China
Authorized Representative
TRANSMEDIC INDONESIAAR Address
Perkantoran Menara Era Unit G-01 JL.Senen Raya No.135-137 RT 00 RW 00, Prov. DKI Jakarta, Kota Jakarta Pusat, Kec. Senen, Kel. Senen
Registration Date
Jan 19, 2025
Expiry Date
Dec 31, 2029
Product Type
Surgical Orthopaedic Equipment
Orthopedic manual surgical instrument.
Non Electromedic Non Sterile
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