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TIANLONG Yellow Fever Virus Nucleic Acid Detection Kit (Fluorescence PCR Method) - Indonesia BPOM Medical Device Registration

TIANLONG Yellow Fever Virus Nucleic Acid Detection Kit (Fluorescence PCR Method) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303420494. The device is manufactured by SUZHOU TIANLONG BIOTECHNOLOGY, CO., LTD from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. INTERSKALA MEDIKA INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : C
TIANLONG Yellow Fever Virus Nucleic Acid Detection Kit (Fluorescence PCR Method)
Analysis ID: AKL 20303420494

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. INTERSKALA MEDIKA INDONESIA

AR Address

Green Sedayu Biz Park Blok DM 9/62, Jalan Daan Mogot Km.18

Registration Date

Oct 08, 2024

Expiry Date

Dec 31, 2026

Product Type

Serological Reagents

Dengue virus nucleic acid amplification test reagents

Invitro Diagnostics

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