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ACER MEDICAL VeriSee DR - Indonesia BPOM Medical Device Registration

ACER MEDICAL VeriSee DR is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21201320247. The device is manufactured by ACER MEDICAL INC. from Taiwan (China), and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. QUALTEK CONSULTANT JAKARTA.

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BPOM Registered
Risk Class Kelas Resiko : C
ACER MEDICAL VeriSee DR
Analysis ID: AKL 21201320247

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

ACER MEDICAL INC.

Country of Origin

Taiwan (China)

Authorized Representative

PT. QUALTEK CONSULTANT JAKARTA

AR Address

Icon Business Park Blok K No 6, BSD City, Kab Tangerang, Banten

Registration Date

Jan 25, 2023

Expiry Date

Oct 19, 2027

Product Type

Diagnostic Eye Equipment

Retinal Diagnostic Software Device

Non Radiation Electromedics

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