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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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BPOM Registered
Risk Class Kelas Resiko : B
IDRA – Dedicated Dry Eye Platform
Analysis ID: AKL 21201023027

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Italy

Authorized Representative

SURGIKA ALKESINDO

AR 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.

Non Radiation Electromedics

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