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Quality Care Suite 2.0 - Indonesia BPOM Medical Device Registration

Quality Care Suite 2.0 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501420109. The device is manufactured by GE MEDICAL SYSTEMS, LLC from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is 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
Quality Care Suite 2.0
Analysis ID: AKL 21501420109

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

GE OPERATIONS INDONESIA

AR Address

South Quarter Tower B, Lantai 18-19, JL. R.A. Kartini Kav. 8, Kelurahan Cilandak Barat, Kecamatan Cilandak, Kota Adm. Jakarta Selatan, Provinsi DKI Jakarta, 12430

Registration Date

Feb 20, 2024

Expiry Date

Sep 25, 2028

Product Type

Diagnostic Radiology Equipment

Medical image management and processing system.

Non Radiation Electromedics

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