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NIDEK Opththalmic Surgical System - Indonesia BPOM Medical Device Registration

NIDEK Opththalmic Surgical System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21201410886. The device is manufactured by NIDEK CO., LTD., HAMACHO PLANT from Japan, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MULYA HUSADA JAYA.

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
NIDEK Opththalmic Surgical System
Analysis ID: AKL 21201410886

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Japan

Authorized Representative

PT. MULYA HUSADA JAYA

AR Address

JALAN KERINCI NO 2A

Registration Date

Dec 26, 2018

Expiry Date

Dec 31, 2023

Product Type

Surgical Eye Equipment

Phacofragmentation system.

Non Radiation Electromedics

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