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MOSPIRE Human Papillomavirus Nucleic Acid Amplification Test Kit - Indonesia BPOM Medical Device Registration

MOSPIRE Human Papillomavirus Nucleic Acid Amplification Test Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20306320173. The device is manufactured by JIANGSU MOLE BIOSCIENCE CO.,LTD from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. GENECRAFT LABS.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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BPOM Registered
Risk Class Kelas Resiko : C
MOSPIRE Human Papillomavirus Nucleic Acid Amplification Test Kit
Analysis ID: AKL 20306320173

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. GENECRAFT LABS

AR Address

Business Park kebon Jeruk Blok F2 No 9 Jl. Meruya Ilir Raya No. 88

Registration Date

Jan 25, 2023

Expiry Date

Dec 31, 2026

Product Type

Tumor Antigen Immunologic Test System

Dna Detection for Human Papillomavirus

Invitro Diagnostics

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DJ Fang

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