JUOSPUR Disposable Virus Specimen Collection Tube - Indonesia BPOM Medical Device Registration
JUOSPUR Disposable Virus Specimen Collection Tube is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10302220224. The device is manufactured by CHANGSA RENJI MEDICAL EQUIPMENT CO., LTD from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. JUOSPUR MULTI PELITA.
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 : 1
Manufacturer
CHANGSA RENJI MEDICAL EQUIPMENT CO., LTDCountry of Origin
China
Authorized Representative
PT. JUOSPUR MULTI PELITAAR Address
JUOSPUR MULTI PELITA
Registration Date
Dec 19, 2022
Expiry Date
Dec 16, 2025
Product Type
Microbiology Equipment
Transport culture medium.
Invitro Diagnostics
RENJI Novel Coronavirus (COVID-19) Nucleic Acid Detection Kit (Real-time RT-PCR Method)
CHANGSHA RENJI MEDICAL EQUIPMENT CO.,LTD.
JUOSPUR Disposable Virus Specimen Collection Tube
CHANGSHA RENJI MEDICAL EQUIPMENT CO.,LTD.
JUOSPUR Disposable Virus Specimen Collection Tube
SHANDONG CHENGWU MEDICAL PRODUCTS FACTORY

