Pure Global

NIDEK Ophthalmic Chair - Indonesia BPOM Medical Device Registration

NIDEK Ophthalmic Chair is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11201917808. The device is manufactured by NIDEK CO., LTD. from Japan, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is 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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : A
NIDEK Ophthalmic Chair
Analysis ID: AKL 11201917808

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

NIDEK CO., LTD.

Country of Origin

Japan

Authorized Representative

MULYA HUSADA JAYA

AR Address

JALAN KERINCI NO. 2-A

Registration Date

Apr 05, 2024

Expiry Date

Mar 31, 2028

Product Type

Diagnostic Eye Equipment

Ophthalmic chair.

Non Electromedic Non Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing