SP3, DiamondGlow ™ - Indonesia BPOM Medical Device Registration
SP3, DiamondGlow ™ is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603220962. The device is manufactured by ZELTIQ AESTHETICS INC from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is REDO MARKETING INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ZELTIQ AESTHETICS INCCountry of Origin
United States
Authorized Representative
REDO MARKETING INDONESIAAR Address
Ruko Renata Jl.Jalur Sutera Timur Blok 1A No. 9 Alam Sutera Kel. Kunciran Kec. Pinang
Registration Date
Sep 03, 2024
Expiry Date
Jul 24, 2029
Product Type
Surgical Equipment
Surgical instrument motors and accessories/attachments.
Non Radiation Electromedics

