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GENEMIND Universal Reaction Kit for Sequencing (Reversible Terminator Sequencing) - Indonesia BPOM Medical Device Registration

GENEMIND Universal Reaction Kit for Sequencing (Reversible Terminator Sequencing) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10204420048. The device is manufactured by GENEMIND BIOSCIENCES CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. 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.

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BPOM Registered
Risk Class Kelas Resiko : A
GENEMIND Universal Reaction Kit for Sequencing (Reversible Terminator Sequencing)
Analysis ID: AKL 10204420048

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

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

Feb 28, 2024

Expiry Date

Oct 11, 2027

Product Type

Reagents and Specimen Providers

General purpose reagent.

Invitro Diagnostics

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