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.
Risk Classification
Product Class
Kelas : 2
Manufacturer
BIONEN S.R.L.Country of Origin
Italy
Authorized Representative
AKSATA MARGA MAKMURAR 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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