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EUROPA All-In-One Solution - Indonesia BPOM Medical Device Registration

EUROPA All-In-One Solution is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21204812770. The device is manufactured by NEO VISION CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. CREATIVE MANAGEMENT OPTICALS.

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 : C
EUROPA All-In-One Solution
Analysis ID: AKL 21204812770

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Korea

Authorized Representative

PT. CREATIVE MANAGEMENT OPTICALS

AR Address

Green Garden Blok A7/25 Jakarta Barat - 11520

Registration Date

Apr 19, 2021

Expiry Date

Apr 16, 2024

Product Type

Therapeutic Eye Equipment

Soft (hydrophilic) contact lens care products.

Non Electromedic Sterile

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