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ARMSTRONG MEDICAL AquaVENT Gas Flow Driver - Indonesia BPOM Medical Device Registration

ARMSTRONG MEDICAL AquaVENT Gas Flow Driver is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403027474. The device is manufactured by ARMSTRONG MEDICAL LIMITED from United Kingdom, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MAIN COMMERCIAL HOSPI.

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BPOM Registered
Risk Class Kelas Resiko : B
ARMSTRONG MEDICAL AquaVENT Gas Flow Driver
Analysis ID: AKL 20403027474

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

United Kingdom

Authorized Representative

PT. MAIN COMMERCIAL HOSPI

AR Address

JL. TAMAN MEKAR AGUNG NO. 32-33 RT.003-RW.006 KEL. MEKARWANGI, KEC. BOJONGLOA KIDUL - KOTA BANDUNG

Registration Date

Nov 29, 2022

Expiry Date

Dec 31, 2025

Product Type

Therapeutic Anesthesia Equipment

High flow humidified oxygen delivery device.

Non Radiation Electromedics

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