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VivaDiag Free Triiodothyronine Test Kit (FIA) - Indonesia BPOM Medical Device Registration

VivaDiag Free Triiodothyronine Test Kit (FIA) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101420397. The device is manufactured by VIVACHEK BIOTECH (HANGZHOU) CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MAIN MEDICAL CHAKRA.

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
VivaDiag Free Triiodothyronine Test Kit (FIA)
Analysis ID: AKL 20101420397

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. MAIN MEDICAL CHAKRA

AR Address

FORESTA BUSINESS LOFT 6 No. 10, Jl. Raya Boulevard Utara BSD City, Desa/Kelurahan Lengkong Kulon

Registration Date

Mar 13, 2024

Expiry Date

Nov 23, 2028

Product Type

Clinical Chemistry Test System

Total triiodothyronine test system (card)

Invitro Diagnostics

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