Optomed Polaris - Indonesia BPOM Medical Device Registration
Optomed Polaris is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21201420023. The device is manufactured by OPTOMED PLC from Finland, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is HARLISA TRUE AWARD.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
OPTOMED PLCCountry of Origin
Finland
Authorized Representative
HARLISA TRUE AWARDAR Address
Jalan Sriti Blok HH-15, Perumahan Sedati Permai
Registration Date
Feb 02, 2024
Expiry Date
Dec 01, 2026
Product Type
Diagnostic Eye Equipment
Opthalmic camera.
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