AMMI CRYSTAL - Indonesia BPOM Medical Device Registration
AMMI CRYSTAL is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602917101. 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 UNIJAYA PRATAMA.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
BIOPLUS, CO. LTDCountry of Origin
Korea
Authorized Representative
UNIJAYA PRATAMAAR Address
JL. PULO KAMBING II KAV.I-22, KAWASAN INDUSTRI PULOGADUNG (JIEP)
Registration Date
Nov 06, 2019
Expiry Date
Jul 31, 2024
Product Type
Prosthetic Surgical Equipment
Dermal filler
Non Electromedic Sterile

