SPIRIT Hammer Percussion - Indonesia BPOM Medical Device Registration
SPIRIT Hammer Percussion is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11001220013. The device is manufactured by CHIN KOU MEDICAL INSTRUMENT CO., LTD. from Taiwan (China), and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. SEKARGUNA MEDIKA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
CHIN KOU MEDICAL INSTRUMENT CO., LTD.Country of Origin
Taiwan (China)
Authorized Representative
PT. SEKARGUNA MEDIKAAR Address
JL. Ciputat Raya Nomor 64
Registration Date
Mar 15, 2023
Expiry Date
Aug 23, 2026
Product Type
Diagnostic Neurology Equipment
Percussor.
Non Electromedic Non Sterile
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