D-ACTOR 100 - Indonesia BPOM Medical Device Registration
D-ACTOR 100 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21403420460. The device is manufactured by STORZ MEDICAL AG from Switzerland, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. AESENDIA INFINI INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
STORZ MEDICAL AGCountry of Origin
Switzerland
Authorized Representative
PT. AESENDIA INFINI INDONESIAAR Address
Business Park Kebon Jeruk Blok D2 No. 10, Jl. Meruya Ilir Raya No. 88
Registration Date
Dec 16, 2024
Expiry Date
Dec 31, 2026
Product Type
Therapeutic Physical Health Equipment
Extracorporeal shock wave treatment device
Non Radiation Electromedics
