MODULO PLUS Electrotherapy - Indonesia BPOM Medical Device Registration
MODULO PLUS Electrotherapy is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21403220020. The device is manufactured by FISIOLINE S.R.L [REGISTER] from Italy, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is HARLISA TRUE AWARD.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
FISIOLINE S.R.L [REGISTER]Country of Origin
Italy
Authorized Representative
HARLISA TRUE AWARDAR Address
Jalan Sriti Blok HH-15, Perumahan Sedati Permai
Registration Date
Jul 29, 2024
Expiry Date
Feb 13, 2027
Product Type
Therapeutic Physical Health Equipment
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