AMMI DIAMOND - Indonesia BPOM Medical Device Registration
AMMI DIAMOND is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602023635. 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., LTD.Country of Origin
Korea
Authorized Representative
PT. UNIJAYA PRATAMAAR Address
JL. PULO KAMBING II KAV.I-22, KAWASAN INDUSTRI PULOGADUNG (JIEP)
Registration Date
Jul 03, 2020
Expiry Date
Apr 14, 2025
Product Type
Prosthetic Surgical Equipment
Dermal filler
Non Electromedic Sterile
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