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SOMATOM go. Sim - Indonesia BPOM Medical Device Registration

SOMATOM go. Sim is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21502122328. The device is manufactured by SIEMENS SHANGHAI MEDICAL EQUIPMENT LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. SIEMENS HEALTHINEERS INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : C
SOMATOM go. Sim

SOMATOM go.Sim

Analysis ID: AKL 21502122328

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. SIEMENS HEALTHINEERS INDONESIA

AR Address

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

Registration Date

Jun 20, 2023

Expiry Date

May 08, 2028

Product Type

Therapeutic Radiology Equipment

Radiation therapy simulation system.

Electromedic Radiation

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