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STANDAREAGEN Diagnostic Kit for Antibody to Human Immunodeficiency Virus HIV 1 + 2 - Indonesia BPOM Medical Device Registration

STANDAREAGEN Diagnostic Kit for Antibody to Human Immunodeficiency Virus HIV 1 + 2 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30305021428. The device is manufactured by NANTONG EGENS BIOTECHNOLOGY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. SARANA KARYA MEDIKA.

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BPOM Registered
Risk Class Kelas Resiko : D
STANDAREAGEN Diagnostic Kit for Antibody to Human Immunodeficiency Virus HIV 1 + 2
Analysis ID: AKL 30305021428

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

China

Authorized Representative

PT. SARANA KARYA MEDIKA

AR Address

UBUD VILLAGE BLOK KINTAMANI C1 NO.15 KEL.SUDIMARA TIMUR

Registration Date

Feb 08, 2023

Expiry Date

Feb 01, 2026

Product Type

Immunological Test System

Multiple autoantibodies immunological test system.

Invitro Diagnostics

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