HYZER ME - Indonesia BPOM Medical Device Registration
HYZER ME is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603023951. The device is manufactured by ILOODA CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is ZHENGAN INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ILOODA CO., LTD.Country of Origin
Korea
Authorized Representative
ZHENGAN INDONESIAAR Address
Ruko Duren Sawit Center No. 8E, Jl. Raya Duren Sawit
Registration Date
Jul 16, 2020
Expiry Date
May 13, 2025
Product Type
Surgical Equipment
Focused ultrasound stimulator system for aesthetic use
Non Radiation Electromedics

