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Bact/Alert 3D 240 - Indonesia BPOM Medical Device Registration

Bact/Alert 3D 240 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10302121004. The device is manufactured by BIOMERIEUX INC. (Missouri) from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. ENSEVAL MEDIKA PRIMA.

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BPOM Registered
Risk Class Kelas Resiko : A
Bact/Alert 3D 240
Analysis ID: AKL 10302121004

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

United States

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

Dec 27, 2024

Expiry Date

Dec 31, 2028

Product Type

Microbiology Equipment

Selective culture medium.

Invitro Diagnostics

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