ALGISCAN Pupillary Algesimeter - Indonesia BPOM Medical Device Registration

ALGISCAN Pupillary Algesimeter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20401220004. The device is manufactured by IDMED from France, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. IDS MEDICAL SYSTEMS INDONESIA.

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BPOM Registered

Risk Class Kelas Resiko : B

ALGISCAN Pupillary Algesimeter

Analysis ID: AKL 20401220004

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

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

Sep 03, 2023

Expiry Date

Dec 31, 2025

Product Type

Diagnostic Anesthesia Equipment

Powered algesimeter.

Non Radiation Electromedics

DJ Fang

MedTech Regulatory Expert

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