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ALLIA IGS 7 - Indonesia BPOM Medical Device Registration

ALLIA IGS 7 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501321418. The device is manufactured by GE MEDICAL SYSTEMS SCS from France, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. GE OPERATIONS 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 : C
ALLIA IGS 7
Analysis ID: AKL 21501321418

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

France

Authorized Representative

PT. GE OPERATIONS INDONESIA

AR Address

South Quarter Tower B, Lt. 18-19, Jl. R.A. Kartini Kav. 8

Registration Date

Sep 03, 2024

Expiry Date

Jun 11, 2026

Product Type

Diagnostic Radiology Equipment

Image-intensified fluoroscopic x-ray system.

Electromedic Radiation

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