Pure Global

INAMI Exophthalmometer - Indonesia BPOM Medical Device Registration

INAMI Exophthalmometer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11201320284. The device is manufactured by INAMI & CO., LTD. from Japan, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is EAST RAYA LESTARI.

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
INAMI Exophthalmometer
Analysis ID: AKL 11201320284

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

INAMI & CO., LTD.

Country of Origin

Japan

Authorized Representative

EAST RAYA LESTARI

AR Address

Jalan Rawa kepiting nomor 4 Kawasan Industri Pulo Gadung Jakarta Timur

Registration Date

Mar 13, 2023

Expiry Date

Jan 11, 2028

Product Type

Diagnostic Eye Equipment

Exophthalmometer.

Non Electromedic Non Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing