Pure Global

GeneMind Fetal Chromosome Aneuploidy Detection Kit (Sequencing Method) - Indonesia BPOM Medical Device Registration

GeneMind Fetal Chromosome Aneuploidy Detection Kit (Sequencing Method) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20204420010. The device is manufactured by GENEMIND BIOSCIENCES CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. GENECRAFT LABS.

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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : B
GeneMind Fetal Chromosome Aneuploidy Detection Kit (Sequencing Method)
Analysis ID: AKL 20204420010

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. GENECRAFT LABS

AR Address

BUSINESS PARK KEBON JERUK BLOK F.2 NO. 9, JL. MERUYA ILIR NO. 88

Registration Date

Jan 21, 2024

Expiry Date

Oct 11, 2027

Product Type

Reagents and Specimen Providers

Analyte specific reagents.

Invitro Diagnostics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing