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BIOPANDA Dengue Combo Rapid Test Cassette - Indonesia BPOM Medical Device Registration

BIOPANDA Dengue Combo Rapid Test Cassette is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303321158. The device is manufactured by BIOPANDA DIAGNOSTICS from United Kingdom, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. BESTARI SUKSES MAKMUR.

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
BIOPANDA Dengue Combo Rapid Test Cassette
Analysis ID: AKL 20303321158

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

United Kingdom

Authorized Representative

PT. BESTARI SUKSES MAKMUR

AR Address

Kokan Permata Kelapa Gading Blok E No. 5 Jl. Boulevard Bukit Gading Raya, Kel. Gading Barat, Kec. Kelapa Gading, Jakarta Utara

Registration Date

May 25, 2023

Expiry Date

Oct 17, 2026

Product Type

Serological Reagents

Dengue virus serological reagents

Invitro Diagnostics

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