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NIDEK Non-Mydriatic Auto Fundus Camera - Indonesia BPOM Medical Device Registration

NIDEK Non-Mydriatic Auto Fundus Camera is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21201410885. The device is manufactured by NIDEK CO., LTD. HAMACO PLAN from Japan, and is classified as Risk Class Kelas Resiko : B. 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 : B
NIDEK Non-Mydriatic Auto Fundus Camera
Analysis ID: AKL 21201410885

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Japan

Authorized Representative

PT. MULYA HUSADA JAYA

AR Address

JALAN KERINCI NO. 2-A

Registration Date

Jan 11, 2024

Expiry Date

Mar 31, 2028

Product Type

Diagnostic Eye Equipment

Opthalmic camera.

Non Radiation Electromedics

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