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BIOSYNEX Ampliquick Fecal Pretreatment - Indonesia BPOM Medical Device Registration

BIOSYNEX Ampliquick Fecal Pretreatment is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10302320346. The device is manufactured by BIOSYNEX SA from France, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. PACIFIC SAINTIFINDO.

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Risk Class Kelas Resiko : A
BIOSYNEX Ampliquick Fecal Pretreatment
Analysis ID: AKL 10302320346

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

BIOSYNEX SA

Country of Origin

France

Authorized Representative

PT. PACIFIC SAINTIFINDO

AR Address

PASIFIK SAINTIFINDO

Registration Date

Aug 24, 2023

Expiry Date

Sep 07, 2024

Product Type

Microbiology Equipment

Transport culture medium.

Invitro Diagnostics

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