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NAMI Contact Lens - Indonesia BPOM Medical Device Registration

NAMI Contact Lens is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21204220300. The device is manufactured by I-ZONE from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. KATAMATA.

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
NAMI Contact Lens
Analysis ID: AKL 21204220300

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

I-ZONE

Country of Origin

Korea

Authorized Representative

PT. KATAMATA

AR Address

Delta Building Blok A/20 Jl. Suryopranoto No. 1

Registration Date

Aug 29, 2022

Expiry Date

Aug 29, 2025

Product Type

Therapeutic Eye Equipment

Soft (hydrophilic) contact lens.

Non Electromedic Sterile

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