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SEINOFY Covid-19 Antigen Rapid Test Cassette - Indonesia BPOM Medical Device Registration

SEINOFY Covid-19 Antigen Rapid Test Cassette is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303126970. The device is manufactured by ZHEJIANG ANJI SAIANFU BIOTECH CO.,LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. JOY INDO 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
SEINOFY Covid-19 Antigen Rapid Test Cassette
Analysis ID: AKL 20303126970

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. JOY INDO MEDIKA

AR Address

JALAN WR SUPRATMAN NOMOR 168

Registration Date

Nov 09, 2022

Expiry Date

Aug 25, 2026

Product Type

Serological Reagents

Respiratory viral panel multiplex nucleic acid assay

Invitro Diagnostics

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