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BIOSCIENCE Novel Coronavirus (2019-nCoV) Antibody Rapid Test - Indonesia BPOM Medical Device Registration

BIOSCIENCE Novel Coronavirus (2019-nCoV) Antibody Rapid Test is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303025893. The device is manufactured by BIOSCIENCE (TIANJIN) DIAGNOSTIC TECHNOLOGY CO.,LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. PRATAMINDO MITRA RIZKY.

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
BIOSCIENCE Novel Coronavirus (2019-nCoV) Antibody Rapid Test
Analysis ID: AKL 20303025893

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. PRATAMINDO MITRA RIZKY

AR Address

Perumahan Bogorami Indah Regency, Jl. Bulak Setro Indah II Blok B 51-52, Surabaya

Registration Date

Oct 17, 2021

Expiry Date

Dec 31, 2024

Product Type

Serological Reagents

Respiratory viral panel multiplex nucleic acid assay

Invitro Diagnostics

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DJ Fang

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