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DIXION Emergency Suction Pump - Indonesia BPOM Medical Device Registration

DIXION Emergency Suction Pump is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603615708. The device is manufactured by DIXION VERTIEB. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. GLOBAL SYSTECH MEDIKA.

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BPOM Registered
Risk Class Kelas Resiko : B
DIXION Emergency Suction Pump
Analysis ID: AKL 21603615708

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

DIXION VERTIEB.

Country of Origin

Germany

Authorized Representative

PT. GLOBAL SYSTECH MEDIKA

AR Address

Jl. TB Simatupang No.17 RT.011/002 Kel. Susukan, Kec. Ciracas Jakarta Timur

Registration Date

Nov 17, 2020

Expiry Date

Nov 12, 2025

Product Type

Surgical Equipment

Powered suction pump.

Non Radiation Electromedics

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