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TYPHIFAST IgM - Indonesia BPOM Medical Device Registration

TYPHIFAST IgM is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303611666. The device is manufactured by AB DIAGNOPATH MANUFACTURING PVT., LTD. from India, and is classified as Risk Class Kelas Resiko : B. 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 : B
TYPHIFAST IgM
Analysis ID: AKL 20303611666

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

India

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

Apr 20, 2021

Expiry Date

May 01, 2024

Product Type

Serological Reagents

Salmonella spp. serological reagents.

Invitro Diagnostics

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