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ANCOOL Ultrasonic Pulmonary Function Testing - Indonesia BPOM Medical Device Registration

ANCOOL Ultrasonic Pulmonary Function Testing is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20401420018. The device is manufactured by ANCOOL TECHNOLOGY CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. INDOPRIMA BIONET.

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BPOM Registered
Risk Class Kelas Resiko : B
ANCOOL Ultrasonic Pulmonary Function Testing
Analysis ID: AKL 20401420018

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. INDOPRIMA BIONET

AR Address

Jalan Tamansari Raya, Komplek 56 No. 56 B Jakarta Barat 11150

Registration Date

May 07, 2024

Expiry Date

Jan 02, 2027

Product Type

Diagnostic Anesthesia Equipment

Diagnostic spirometer.

Non Radiation Electromedics

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DJ Fang

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