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VITEK DENSICHEK and Accessories - Indonesia BPOM Medical Device Registration

VITEK DENSICHEK and Accessories is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20301220007. The device is manufactured by BIOMERIEUX INC., (Missouri) 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 DENSICHEK and Accessories
Analysis ID: AKL 20301220007

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

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

Nov 06, 2024

Expiry Date

Dec 31, 2028

Product Type

Diagnostic Equipment

Fully automated short-term incubation cycle antimicrobial susceptibility system.

Invitro Diagnostics

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