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NEUROCONN Thera Prax Q EEG - Indonesia BPOM Medical Device Registration

NEUROCONN Thera Prax Q EEG is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21003615841. The device is manufactured by NEUROCONN GMBH. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. KARINDO ALKESTRON.

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BPOM Registered
Risk Class Kelas Resiko : B
NEUROCONN Thera Prax Q EEG
Analysis ID: AKL 21003615841

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

NEUROCONN GMBH.

Country of Origin

Germany

Authorized Representative

PT. KARINDO ALKESTRON

AR Address

JL. TOMANG RAYA NO.17

Registration Date

Dec 01, 2020

Expiry Date

Jul 13, 2025

Product Type

Therapeutic Neurology Equipment

Biofeedback device.

Non Radiation Electromedics

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