QIAscreen HPV PCR Test - Indonesia BPOM Medical Device Registration
QIAscreen HPV PCR Test is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20306026110. The device is manufactured by LABO BIO-MEDICAL PRODUCTS from Netherlands, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. UBC MEDICAL INDONESIA.
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.
Risk Classification
Product Class
Kelas : 2
Manufacturer
LABO BIO-MEDICAL PRODUCTSCountry of Origin
Netherlands
Authorized Representative
PT. UBC MEDICAL INDONESIAAR Address
Jalan Rawa Gelam V, Blok L Kav. 11-13, Kawasan Industri Pulogadung Jakarta Timur13930
Registration Date
Oct 13, 2020
Expiry Date
Jul 25, 2024
Product Type
Tumor Antigen Immunologic Test System
Dna Detection for Human Papillomavirus
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