Pure Global

ZEESAN SARS-CoV-2 Test Kit (Real-Time PCR) - Indonesia BPOM Medical Device Registration

ZEESAN SARS-CoV-2 Test Kit (Real-Time PCR) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303025896. The device is manufactured by XIAMEN ZEESAN BIOTECH CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. FAITHFUL MEDICAL GRACE.

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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : B
ZEESAN SARS-CoV-2 Test Kit (Real-Time PCR)
Analysis ID: AKL 20303025896

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. FAITHFUL MEDICAL GRACE

AR Address

Mitra Sunter Boulevard Blok B No.39 Jl. Yos Sudarso Kav. 89

Registration Date

Feb 06, 2023

Expiry Date

Jun 06, 2027

Product Type

Serological Reagents

Respiratory viral panel multiplex nucleic acid assay

Invitro Diagnostics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Other Products from XIAMEN ZEESAN BIOTECH CO., LTD
Products from the same manufacturer (2 products)