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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.

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BPOM Registered
Risk Class Kelas Resiko : B
OPTOMED Smartscope FA Plus
Analysis ID: AKL 21201220042

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

OPTOMED OY

Country of Origin

Finland

Authorized Representative

PT. EAST RAYA LESTARI

AR 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

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