OPTOMED Smartscope FA Plus - Indonesia BPOM Medical Device Registration
OPTOMED Smartscope FA Plus is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21201220042. The device is manufactured by OPTOMED OY from Finland, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. EAST RAYA LESTARI.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
Risk Classification
Product Class
Kelas : 2
Manufacturer
OPTOMED OYCountry of Origin
Finland
Authorized Representative
PT. EAST RAYA LESTARIAR Address
Jl. Rawa Kepiting No. 4, Kawasan Industri Pulogadung
Registration Date
Feb 01, 2025
Expiry Date
Jan 18, 2026
Product Type
Diagnostic Eye Equipment
Opthalmic camera.
Non Radiation Electromedics
UNICOS Visual Ophthalmic Projector
UNIQUE CO., LTD.
UNICOS Autorefkeratometer System Set
UNIQUE CO., LTD.
UNICOS Integrated Refraction System
UNIQUE CO., LTD.
UNICOS Ophthalmic Integrated Refraction System Chair
UNIQUE CO., LTD.
UNIQUE Auto Refractory - Keratometer
UNIQUE CO., LTD.
UNICOS LCD Chart
UNIQUE CO., LTD.
UNICOS Auto Refracto Keratometer 3D
UNIQUE CO., LTD.
UNICOS Auto Chart Projector
UNIQUE CO., LTD.
UNICOS Digital Refractor (Phoroptor)
UNIQUE CO., LTD.
RAY VISION Instrument Table
66 VISION TECH CO., LTD

