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FRESHKON Clear Multipurpose Solution - Indonesia BPOM Medical Device Registration

FRESHKON Clear Multipurpose Solution is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21204918769. The device is manufactured by YUNG SHENG OPTICAL CO., LTD. from Taiwan (China), and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. OCULUS INDONESIA.

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
FRESHKON Clear Multipurpose Solution
Analysis ID: AKL 21204918769

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Taiwan (China)

Authorized Representative

PT. OCULUS INDONESIA

AR Address

Jl. Pembangunan ll No. 16 K - Jakarta Pusat

Registration Date

May 16, 2024

Expiry Date

Apr 16, 2029

Product Type

Therapeutic Eye Equipment

Soft (hydrophilic) contact lens care products.

Non Electromedic Sterile

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