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GALENUS Dengue NS1 Rapid Test (Colloidal Gold) - Indonesia BPOM Medical Device Registration

GALENUS Dengue NS1 Rapid Test (Colloidal Gold) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303420394. The device is manufactured by TIANJIN GALENUS MEDICAL CO.,LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. INNOVATION HEALTHCARE INDONESIA.

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 : C
GALENUS Dengue NS1 Rapid Test (Colloidal Gold)
Analysis ID: AKL 20303420394

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. INNOVATION HEALTHCARE INDONESIA

AR Address

Komplek Ruko Permata Kota, Blok Q No. 11 Jl. Pangeran Tubagus Angke No. 170 Kel. Penjagalan, Kec. Penjaringan, Jakarta Utara 14450

Registration Date

Aug 26, 2024

Expiry Date

Feb 05, 2027

Product Type

Serological Reagents

Dengue virus serological reagents

Invitro Diagnostics

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