Acuson X700 - Indonesia BPOM Medical Device Registration

Acuson X700 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501321037. The device is manufactured by SIEMENS HEALTHINEERS LTD. from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is SIEMENS HEALTHINEERS INDONESIA.

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BPOM Registered

Risk Class Kelas Resiko : B

Acuson X700

Analysis ID: AKL 21501321037

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

SIEMENS HEALTHINEERS LTD.

Country of Origin

Korea

Authorized Representative

SIEMENS HEALTHINEERS INDONESIA

AR Address

Perkantoran Hijau Arkadia Tower F, Lantai 18, Jl. Tahi Bonar Simatupang Kav. 88, Kel. Kebagusan, Kec. Pasar Minggu, Jakarta Selatan, DKI Jakarta

Registration Date

Jun 16, 2023

Expiry Date

Jul 25, 2027

Product Type

Diagnostic Radiology Equipment

Ultrasonic pulsed doppler imaging system.

Non Radiation Electromedics

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Acuson X700 - Indonesia BPOM Medical Device Registration

Risk Classification

Product Class

Manufacturer

Country of Origin

Authorized Representative

AR Address

Registration Date

Expiry Date

Product Type

DJ Fang

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