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VIDAS Kube Clinical - Indonesia BPOM Medical Device Registration

VIDAS Kube Clinical is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20304320179. The device is manufactured by BIOMERIEUX ITALIA S.P.A. from Italy, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ENSEVAL MEDIKA PRIMA.

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
VIDAS Kube Clinical
Analysis ID: AKL 20304320179

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Italy

Authorized Representative

PT. ENSEVAL MEDIKA PRIMA

AR Address

JL. PULO LENTUT NO.12, LT.1 UNIT 1C & LT.2 UNIT 2A, KAWASAN INDUSTRI PULOGADUNG

Registration Date

Jul 24, 2024

Expiry Date

Dec 31, 2026

Product Type

Immunology Laboratory Equipment and Reagents

Immunofluorometer equipment

Invitro Diagnostics

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