CELLUMA RESTORE - Indonesia BPOM Medical Device Registration
CELLUMA RESTORE is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21403320872. The device is manufactured by BIOPHOTAS, INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. REDO MARKETING INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
BIOPHOTAS, INC.Country of Origin
United States
Authorized Representative
PT. REDO MARKETING INDONESIAAR Address
Ruko Renata Jl.Jalur Sutera Timur Blok 1A No. 9 Alam Sutera Kel. Kunciran Kec. Pinang
Registration Date
Nov 28, 2023
Expiry Date
Aug 16, 2028
Product Type
Therapeutic Physical Health Equipment
Infrared lamp.
Non Radiation Electromedics
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