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 21501022270. The device is manufactured by SIEMENS HEALTHINEERS AG from Germany, 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 21501022270

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

SIEMENS HEALTHINEERS AG

Country of Origin

Germany

Authorized Representative

SIEMENS HEALTHINEERS INDONESIA

AR Address

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

Registration Date

Nov 17, 2024

Expiry Date

Mar 27, 2028

Product Type

Diagnostic Radiology Equipment

Magnetic resonance diagnostic device.

Non Radiation Electromedics

DJ Fang

MedTech Regulatory Expert

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