PRODEFINE Ultra Deep - Indonesia BPOM Medical Device Registration
PRODEFINE Ultra Deep is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602320173. The device is manufactured by LIFE S.R.L from Italy, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. UNISON MEDIKA JAYA.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
LIFE S.R.LCountry of Origin
Italy
Authorized Representative
PT. UNISON MEDIKA JAYAAR Address
JALAN GUNTUR NOMOR 7, RT. 013, RW. 005, KEL. PASAR MANGGIS, KEC. SETIABUDI, JAKARTA SELATAN.
Registration Date
Mar 25, 2023
Expiry Date
Mar 15, 2027
Product Type
Prosthetic Surgical Equipment
Dermal filler
Non Electromedic Sterile
