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PHILIPS CT 5300 - Indonesia BPOM Medical Device Registration

PHILIPS CT 5300 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501420644. 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 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 CT 5300
Analysis ID: AKL 21501420644

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PHILIPS INDONESIA COMMERCIAL

AR Address

Gedung Cibis Nine Lantai 10, Jl. T.B. Simatupang No. 2 RT 001 RW 005

Registration Date

Sep 23, 2024

Expiry Date

May 14, 2029

Product Type

Diagnostic Radiology Equipment

Computed tomography x-ray system.

Electromedic Radiation

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