VivaDiag Anti-Mullerian Hormone Test Kit (FIA) - Indonesia BPOM Medical Device Registration

VivaDiag Anti-Mullerian Hormone Test Kit (FIA) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101324278. 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 CAKRA MEDIKA UTAMA.

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BPOM Registered

Risk Class Kelas Resiko : B

VivaDiag Anti-Mullerian Hormone Test Kit (FIA)

Analysis ID: AKL 20101324278

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

VIVACHEK BIOTECH (HANGZHOU) CO., LTD.

Country of Origin

China

Authorized Representative

CAKRA MEDIKA UTAMA

AR Address

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

Registration Date

Nov 17, 2023

Expiry Date

Sep 10, 2025

Product Type

Clinical Chemistry Test System

Anti-Mullerian Hormone Test System (card)

Invitro Diagnostics

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Other Products from VIVACHEK BIOTECH (HANGZHOU) CO., LTD.

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VivaDiag Anti-Mullerian Hormone Test Kit (FIA) - Indonesia BPOM Medical Device Registration

Risk Classification

Product Class

Manufacturer

Country of Origin

Authorized Representative

AR Address

Registration Date

Expiry Date

Product Type

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