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BIOIC Allergen Specific-IgE Detection kit - Indonesia BPOM Medical Device Registration

BIOIC Allergen Specific-IgE Detection kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20305713229. The device is manufactured by AGNITIO SCIENCE AND TECHNOLOGY, INC. from Taiwan (China), and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. INDOLABTEK DYNAMICS.

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
BIOIC Allergen Specific-IgE Detection kit
Analysis ID: AKL 20305713229

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Taiwan (China)

Authorized Representative

PT. INDOLABTEK DYNAMICS

AR Address

Rukan Royal Palace B-25. JL. Prof. Dr. Soepomo. SH, No. 178A. Menteng Dalam. Jakarta Selatan.

Registration Date

Jul 29, 2024

Expiry Date

Jul 01, 2029

Product Type

Immunological Test System

Immunoglobulins A, G, M, D, and E immunological test system.

Invitro Diagnostics

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