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BIOMERIEUX Brucella Blood Agar (BBA) - Indonesia BPOM Medical Device Registration

BIOMERIEUX Brucella Blood Agar (BBA) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10302420043. The device is manufactured by BIOMERIEUX ESPANA S.A, SPAIN from Spain, and is classified as Risk Class Kelas Resiko : A. 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 : A
BIOMERIEUX Brucella Blood Agar (BBA)
Analysis ID: AKL 10302420043

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Spain

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

Mar 19, 2024

Expiry Date

Dec 31, 2026

Product Type

Microbiology Equipment

Enriched culture medium.

Invitro Diagnostics

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