PRODIVA 1.5T CX - Indonesia BPOM Medical Device Registration

PRODIVA 1.5T CX is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501816716. The device is manufactured by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. from Netherlands, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. PHILIPS INDONESIA COMMERCIAL.

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BPOM Registered

Risk Class Kelas Resiko : C

PRODIVA 1.5T CX

Analysis ID: AKL 21501816716

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Country of Origin

Netherlands

Authorized Representative

PT. PHILIPS INDONESIA COMMERCIAL

AR Address

Gedung Cibis Nine Lantai 10, Jl. TB Simatupang No. 2

Registration Date

Apr 28, 2023

Expiry Date

May 24, 2027

Product Type

Diagnostic Radiology Equipment

Magnetic resonance diagnostic device.

Non Radiation Electromedics

DJ Fang

MedTech Regulatory Expert

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