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CFX Opus 384 Dx - Indonesia BPOM Medical Device Registration

CFX Opus 384 Dx is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20102420363. The device is manufactured by BIO-RAD LABORATORIES (SINGAPORE) PTE LTD from Singapore, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is ANDAMAN MEDICAL INDONESIA.

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
CFX Opus 384 Dx
Analysis ID: AKL 20102420363

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Singapore

Authorized Representative

ANDAMAN MEDICAL INDONESIA

AR Address

Menara Cardig Lantai 1, Jalan Raya Halim Perdanakusuma

Registration Date

Nov 01, 2024

Expiry Date

Aug 12, 2029

Product Type

Clinical Laboratory Equipment

Instrumentation for clinical multiplex test systems.

Invitro Diagnostics

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