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VITEK MS Prime and Accessories - Indonesia BPOM Medical Device Registration

VITEK MS Prime and Accessories is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20301320082. The device is manufactured by KMC SYSTEMS, INC. from United States, 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
VITEK MS Prime and Accessories
Analysis ID: AKL 20301320082

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

KMC SYSTEMS, INC.

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

Feb 17, 2023

Expiry Date

Dec 31, 2026

Product Type

Serological Reagents

Mass spectrometer system for clinical use for the identification of microorganism

Invitro Diagnostics

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