GENEX - Indonesia BPOM Medical Device Registration
GENEX is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21302321042. The device is manufactured by BIOCOMPOSITES LTD. from United Kingdom, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ASIA ACTUAL INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
BIOCOMPOSITES LTD.Country of Origin
United Kingdom
Authorized Representative
PT. ASIA ACTUAL INDONESIAAR Address
PERKANTORAN GANDARIA 8 LANTAI 6 UNIT JL. SULTAN ISKANDAR MUDA KEBAYORAN LAMA UTARA JAKARTA SELATAN
Registration Date
Dec 14, 2023
Expiry Date
Sep 17, 2028
Product Type
Prosthetic Orthopedic Equipment
Resorbable calcium salt bone void filler device.
Non Electromedic Sterile
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