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ALINITY i Sirolimus Whole Blood Precipitation Reagent - Indonesia BPOM Medical Device Registration

ALINITY i Sirolimus Whole Blood Precipitation Reagent is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20103027685. The device is manufactured by FUJIREBIO DIAGNOSTICS, INC from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ABBOTT PRODUCTS INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : C
ALINITY i Sirolimus Whole Blood Precipitation Reagent
Analysis ID: AKL 20103027685

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

PT. ABBOTT PRODUCTS INDONESIA

AR Address

WISMA PONDOK INDAH 2 SUITE 1000, JL. SULTAN ISKANDAR MUDA KAV. V-TA

Registration Date

Dec 10, 2020

Expiry Date

Aug 06, 2025

Product Type

Clinical Toxicology Test System

Sirolimus test system (kit & cair)

Invitro Diagnostics

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