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MIMI Princess Series Soft Contact Lens, Daily Wear - Indonesia BPOM Medical Device Registration

MIMI Princess Series Soft Contact Lens, Daily Wear is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21204420301. The device is manufactured by GEO MEDICAL CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MULTINDO JAYA RAYA.

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
MIMI Princess Series Soft Contact Lens, Daily Wear
Analysis ID: AKL 21204420301

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Korea

Authorized Representative

PT. MULTINDO JAYA RAYA

AR Address

Jl. Dr. Wahidin Sudiro Husodo Nomor 10, RT.001/RW.005, Kel. Pattunuang, Kec. Wajo, Kota Makassar, Prov. Sulawesi Selatan

Registration Date

Jul 09, 2024

Expiry Date

Feb 01, 2029

Product Type

Therapeutic Eye Equipment

Soft (hydrophilic) contact lens.

Non Electromedic Sterile

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