AMMI AQUA - Indonesia BPOM Medical Device Registration
AMMI AQUA is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602917420. The device is manufactured by BIOPLUS, CO. LTD from Korea, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. UNIJAYA PRATAMA.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
BIOPLUS, CO. LTDCountry of Origin
Korea
Authorized Representative
PT. UNIJAYA PRATAMAAR Address
JL. PULO KAMBING II KAV.I-22, KAWASAN INDUSTRI PULOGADUNG (JIEP)
Registration Date
Dec 09, 2019
Expiry Date
Jul 31, 2024
Product Type
Prosthetic Surgical Equipment
Dermal filler
Non Electromedic Sterile
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