MAGNETOM Lumina - Indonesia BPOM Medical Device Registration

MAGNETOM Lumina is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501220352. The device is manufactured by SIEMENS SHENZHEN MAGNETIC RESONANCE LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is SIEMENS HEALTHINEERS INDONESIA.

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BPOM Registered

Risk Class Kelas Resiko : C

MAGNETOM Lumina

Analysis ID: AKL 21501220352

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

SIEMENS SHENZHEN MAGNETIC RESONANCE LTD.

Country of Origin

China

Authorized Representative

SIEMENS HEALTHINEERS INDONESIA

AR Address

Perkantoran Hijau Arkadia Tower F, Lantai 18, Jl.Tahi Bonar Simatupang Kav. 88

Registration Date

Dec 02, 2024

Expiry Date

Oct 14, 2029

Product Type

Diagnostic Radiology Equipment

Magnetic resonance diagnostic device.

Non Radiation Electromedics

DJ Fang

MedTech Regulatory Expert

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