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PHILIPS Brilliance CT Big Bore - Indonesia BPOM Medical Device Registration

PHILIPS Brilliance CT Big Bore is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501515381. The device is manufactured by PHILIPS HEALTHCARE (SUZHOU) CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. PHILIPS INDONESIA COMMERCIAL.

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
PHILIPS Brilliance CT Big Bore
Analysis ID: AKL 21501515381

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. PHILIPS INDONESIA COMMERCIAL

AR Address

Gedung Cibis Nine Lantai 10 Jl. TB Simatupang No. 2 RT.001 RW. 005 Kel. Cilandak Timur Kec. Pasar Minggu Jakarta Selatan

Registration Date

Oct 07, 2019

Expiry Date

Feb 14, 2024

Product Type

Diagnostic Radiology Equipment

Computed tomography x-ray system.

Electromedic Radiation

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