PHYSIOMED MAGCELL ARTHRO - Indonesia BPOM Medical Device Registration
PHYSIOMED MAGCELL ARTHRO is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21403220228. The device is manufactured by PHYSIOMED ELEKTROMEDIZIN AG. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ANDINI SARANA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
PHYSIOMED ELEKTROMEDIZIN AG.Country of Origin
Germany
Authorized Representative
PT. ANDINI SARANAAR Address
Jln. Rawa Sumur III, Kav. III, Blok DD No. 11. Kawasan Industri Pulogadung Jakarta Timur
Registration Date
Aug 25, 2022
Expiry Date
Mar 28, 2026
Product Type
Therapeutic Physical Health Equipment
Powered muscle stimulator.
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