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DIAGCOR Genoflow HPV Array Test kit - Indonesia BPOM Medical Device Registration

DIAGCOR Genoflow HPV Array Test kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20305810249. The device is manufactured by DIAGCOR BIOSCIENCE INCORPORATION LIMITED from Hong Kong (China), and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. PROSPEROUS ADVANCED ERA.

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
DIAGCOR Genoflow HPV Array Test kit
Analysis ID: AKL 20305810249

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Hong Kong (China)

Authorized Representative

PT. PROSPEROUS ADVANCED ERA

AR Address

RUKO PURI BOTANICAL MEGA KEBON JERUK H.7 NO.17

Registration Date

Dec 18, 2023

Expiry Date

Dec 31, 2026

Product Type

Tumor Antigen Immunologic Test System

Dna Detection for Human Papillomavirus

Invitro Diagnostics

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