DORNIER Aries 2 - Indonesia BPOM Medical Device Registration
DORNIER Aries 2 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31403320556. The device is manufactured by DORNIER MEDTECH SYSTEMS GMBH from Germany, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. INDOMEDIK NIAGA PERKASA.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
DORNIER MEDTECH SYSTEMS GMBHCountry of Origin
Germany
Authorized Representative
PT. INDOMEDIK NIAGA PERKASAAR Address
Jl. Raya Kebayoran Lama No.35 RT.008 RW.001 Kelurahan Sukabumi Selatan, Kecamatan Kebon Jeruk, Jakarta Barat, DKI Jakarta
Registration Date
Jun 04, 2023
Expiry Date
Mar 31, 2027
Product Type
Therapeutic Physical Health Equipment
Extracorporeal shock wave treatment device
Non Radiation Electromedics
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