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NEUROLIGHT Portable Pupillometer - Indonesia BPOM Medical Device Registration

NEUROLIGHT Portable Pupillometer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11201026789. The device is manufactured by IDMED from France, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. IDS MEDICAL SYSTEMS INDONESIA.

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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Risk Class Kelas Resiko : A
NEUROLIGHT Portable Pupillometer
Analysis ID: AKL 11201026789

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

IDMED

Country of Origin

France

Authorized Representative

PT. IDS MEDICAL SYSTEMS INDONESIA

AR Address

Gedung Wisma 76, Lantai 17 & 22, Jl. LetJend. S. Parman Kav.76, Kelurahan Slipi, Kecamatan Palmerah, 11410

Registration Date

Nov 10, 2020

Expiry Date

Dec 31, 2023

Product Type

Diagnostic Eye Equipment

Pupillometer.

Non Radiation Electromedics

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