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InviMag® Universal Kit / KF96 - Indonesia BPOM Medical Device Registration

InviMag® Universal Kit / KF96 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10204220293. The device is manufactured by INVITEK MOLECULAR GMBH from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is SEGMED DISTRIBUTION INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : A
InviMag® Universal Kit / KF96
Analysis ID: AKL 10204220293

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Germany

Authorized Representative

SEGMED DISTRIBUTION INDONESIA

AR Address

SEGMED DISTRIBUSI INDONESIA

Registration Date

Oct 20, 2022

Expiry Date

May 01, 2024

Product Type

Reagents and Specimen Providers

General purpose reagent.

Invitro Diagnostics

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