IDRA – Dedicated Dry Eye Platform - Indonesia BPOM Medical Device Registration
IDRA – Dedicated Dry Eye Platform is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21201023027. The device is manufactured by SBM SISTEMI S. R. L from Italy, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is SURGIKA ALKESINDO.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SBM SISTEMI S. R. LCountry of Origin
Italy
Authorized Representative
SURGIKA ALKESINDOAR Address
Jl. Letjen Suprapto No.60, Gedung Indra Sentral unit G-H, Cempaka Putih
Registration Date
Feb 06, 2025
Expiry Date
Jan 27, 2027
Product Type
Diagnostic Eye Equipment
AC-powered slitlamp biomicroscope.
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