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YANENG Human Papillomavirus Nucleic Acid Detection and HPV16/18 Genotyping Kit (PCR-Fluorescence Probing) - Indonesia BPOM Medical Device Registration

YANENG Human Papillomavirus Nucleic Acid Detection and HPV16/18 Genotyping Kit (PCR-Fluorescence Probing) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20306420168. The device is manufactured by YANENG BIOSCIENCE (SHENZHEN) CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. NALEYA GENOMIK INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : C
YANENG Human Papillomavirus Nucleic Acid Detection and HPV16/18 Genotyping Kit (PCR-Fluorescence Probing)
Analysis ID: AKL 20306420168

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. NALEYA GENOMIK INDONESIA

AR Address

Wisma MRA Lantai 18, Jalan TB. Simatupang Nomor 19

Registration Date

Sep 19, 2024

Expiry Date

Jan 31, 2027

Product Type

Tumor Antigen Immunologic Test System

Dna Detection for Human Papillomavirus

Invitro Diagnostics

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