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EUROCLINIC Vestibular Vibrator - Indonesia BPOM Medical Device Registration

EUROCLINIC Vestibular Vibrator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21001810503. The device is manufactured by MEDI-CARE SOLUTIONS S.R.L. from Italy, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MEGA PRATAMA MEDICALINDO.

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
EUROCLINIC Vestibular Vibrator
Analysis ID: AKL 21001810503

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Italy

Authorized Representative

PT. MEGA PRATAMA MEDICALINDO

AR Address

Jl. Pluit Raya 133 Blok A.3

Registration Date

Feb 19, 2021

Expiry Date

Nov 13, 2025

Product Type

Diagnostic Neurology Equipment

Evoked response auditory stimulator.

Non Radiation Electromedics

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