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BIOMERIEUX Mueller Hinton 2 Gelose/Agar (MH2-D) - Indonesia BPOM Medical Device Registration

BIOMERIEUX Mueller Hinton 2 Gelose/Agar (MH2-D) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20301803240. The device is manufactured by BIOMERIEUX SA. (Craponne) from France, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ENSEVAL MEDIKA PRIMA.

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BPOM Registered
Risk Class Kelas Resiko : B
BIOMERIEUX Mueller Hinton 2 Gelose/Agar (MH2-D)
Analysis ID: AKL 20301803240

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

France

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

Sep 23, 2024

Expiry Date

Dec 31, 2028

Product Type

Diagnostic Equipment

Culture medium for antimicrobial susceptibility tests.

Invitro Diagnostics

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