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Zybio Hepatitis B Virus Nucleic Acid Quantitative Detection Kit (PCR-Fluorescent Probe Method) - Indonesia BPOM Medical Device Registration

Zybio Hepatitis B Virus Nucleic Acid Quantitative Detection Kit (PCR-Fluorescent Probe Method) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30305220626. The device is manufactured by ZYBIO INC. from China, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. ZYBIO MEDICAL INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : D
Zybio Hepatitis B Virus Nucleic Acid Quantitative Detection Kit (PCR-Fluorescent Probe Method)
Analysis ID: AKL 30305220626

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Manufacturer

ZYBIO INC.

Country of Origin

China

Authorized Representative

PT. ZYBIO MEDICAL INDONESIA

AR Address

MGK office tower B, lantai 8, Unit 8B, Jl, Angkasa Kavling B-6, Kota Adm, Jakarta Pusat, Provinsi DKI Jakarta 10610

Registration Date

Dec 21, 2022

Expiry Date

Jan 03, 2027

Product Type

Immunological Test System

Antinuclear antibody immunological test system.

Invitro Diagnostics

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