PRODEFINE RETOUCH - Indonesia BPOM Medical Device Registration
PRODEFINE RETOUCH is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602320269. 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
Jl. Guntur No. 7 RT.013/RW.005, Desa/Kelurahan Pasar Manggis, Kec. Setiabudi, Kota Adm. Jakarta Selatan, Provinsi DKI Jakarta
Registration Date
Sep 21, 2023
Expiry Date
Feb 15, 2028
Product Type
Prosthetic Surgical Equipment
Dermal filler
Non Electromedic Sterile
