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MENICON Z E-1 - Indonesia BPOM Medical Device Registration

MENICON Z E-1 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21204814439. The device is manufactured by MENICON CO. LTD, SEKI PLANT from Japan, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is ALFA INTERNAL OPTINDO.

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
MENICON Z E-1
Analysis ID: AKL 21204814439

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Japan

Authorized Representative

ALFA INTERNAL OPTINDO

AR Address

JALAN KAREL SATSUIT TUBUN NOMOR 72 LANTAI 1 RT.001 / RW.001

Registration Date

Jun 24, 2024

Expiry Date

Dec 31, 2026

Product Type

Therapeutic Eye Equipment

Rigid gas permeable contact lens for daily wear only.

Non Electromedic Sterile

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