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WIZ BIOTECH SARS-CoV-2 Antigen Rapid Test - Indonesia BPOM Medical Device Registration

WIZ BIOTECH SARS-CoV-2 Antigen Rapid Test is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303027922. The device is manufactured by XIAMEN WIZ BIOTECH CO.,LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is MULTI SARANA MEDIKA.

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 : B
WIZ BIOTECH SARS-CoV-2 Antigen Rapid Test
Analysis ID: AKL 20303027922

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

MULTI SARANA MEDIKA

AR Address

Komp. Gading Bukit Indah Jl. Bukit Gading Raya Blok B Kav. No.1

Registration Date

Jun 07, 2023

Expiry Date

Apr 19, 2028

Product Type

Serological Reagents

Respiratory viral panel multiplex nucleic acid assay

Invitro Diagnostics

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DJ Fang

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