BIOFIX - Indonesia BPOM Medical Device Registration
BIOFIX is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31302026319. The device is manufactured by SYNIMED (SYNERGIE INGENIERIE MEDICALE) from France, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. BIOTECH INTI KORPORINDO.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
SYNIMED (SYNERGIE INGENIERIE MEDICALE)Country of Origin
France
Authorized Representative
PT. BIOTECH INTI KORPORINDOAR Address
Komplek Duta Merlin Blok D11-13 lantai 2 Jl. Gajah Mada No 3-5
Registration Date
Nov 16, 2022
Expiry Date
Sep 21, 2026
Product Type
Prosthetic Orthopedic Equipment
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