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BIONEN EEG Prewired Headcaps - Indonesia BPOM Medical Device Registration

BIONEN EEG Prewired Headcaps is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21001520006. The device is manufactured by BIONEN S.R.L. from Italy, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is AKSATA MARGA MAKMUR.

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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BPOM Registered
Risk Class Kelas Resiko : B
BIONEN EEG Prewired Headcaps
Analysis ID: AKL 21001520006

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

BIONEN S.R.L.

Country of Origin

Italy

Authorized Representative

AKSATA MARGA MAKMUR

AR Address

Foresta Business Loft 6 Unit 1, BSD City

Registration Date

Feb 08, 2025

Expiry Date

Mar 13, 2028

Product Type

Diagnostic Neurology Equipment

Cutaneous electrode.

Non Electromedic Non Sterile

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