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AIM Rapid Test TSH-F - Indonesia BPOM Medical Device Registration

AIM Rapid Test TSH-F is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101422206. The device is manufactured by HANGZHOU ALLTEST BIOTECH CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ACCURATE INTAN MADYA.

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
AIM Rapid Test TSH-F
Analysis ID: AKL 20101422206

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. ACCURATE INTAN MADYA

AR Address

KOMPLEK DUTA MERLIN, BLOK. F5 & F6, JL. GAJAH MADA NO. 3-5

Registration Date

Oct 29, 2024

Expiry Date

Oct 19, 2027

Product Type

Clinical Chemistry Test System

Thyroid stimulating hormone test system (card)

Invitro Diagnostics

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