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GENEXUS™ Dx Consumables - Indonesia BPOM Medical Device Registration

GENEXUS™ Dx Consumables is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10102420067. The device is manufactured by LIFE TECHNOLOGIES CORPORATION from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. MURSMEDIC.

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
GENEXUS™ Dx Consumables
Analysis ID: AKL 10102420067

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

United States

Authorized Representative

PT. MURSMEDIC

AR Address

The Kensington Office Tower Lantai 11, Jalan Boulevard Raya Nomor 1, Desa/Kelurahan Kelapa Gading Timur, Kec. Kelapa Gading, Kota Adm. Jakarta Utara, Provinsi DKI Jakarta, 14240

Registration Date

Mar 15, 2024

Expiry Date

Nov 28, 2028

Product Type

Clinical Laboratory Equipment

General purpose laboratory equipment labeled or promoted for a specific medical use.

Invitro Diagnostics

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