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OPTOMED Ophthalmic Camera Aurora - Indonesia BPOM Medical Device Registration

OPTOMED Ophthalmic Camera Aurora is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21201127495. 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 Ophthalmic Camera Aurora
Analysis ID: AKL 21201127495

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

OPTOMED OY

Country of Origin

Finland

Authorized Representative

PT. EAST RAYA LESTARI

AR Address

Jalan Rawa kepiting nomor 4 Kawasan Industri Pulo Gadung Jakarta Timur

Registration Date

Feb 09, 2022

Expiry Date

Jan 18, 2026

Product Type

Diagnostic Eye Equipment

Opthalmic camera.

Non Radiation Electromedics

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