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InBios DENV™ Detect IgM Capture ELISA - Indonesia BPOM Medical Device Registration

InBios DENV™ Detect IgM Capture ELISA is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303420080. The device is manufactured by INBIOS INTERNATIONAL, INC from United States, 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
InBios DENV™ Detect IgM Capture ELISA
Analysis ID: AKL 20303420080

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

PT. BESTARI SUKSES MAKMUR

AR Address

KOKAN PERMATA KELAPA GADING LT. 3, BLOK E-5, JL. BOULEVARD GADING RAYA, KELAPA GADING BARAT, KELAPA GADING, JAKARTA UTARA

Registration Date

Mar 13, 2024

Expiry Date

Apr 17, 2027

Product Type

Serological Reagents

Dengue virus serological reagents

Invitro Diagnostics

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