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IDMED - AlgiScan Pupillary Algesimeter - Indonesia BPOM Medical Device Registration

IDMED - AlgiScan Pupillary Algesimeter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20401719142. 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
IDMED - AlgiScan Pupillary Algesimeter
Analysis ID: AKL 20401719142

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

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

Oct 08, 2020

Expiry Date

Dec 31, 2023

Product Type

Diagnostic Anesthesia Equipment

Powered algesimeter.

Non Radiation Electromedics

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