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APEX DIGIFLOW Uroflometry System - Indonesia BPOM Medical Device Registration

APEX DIGIFLOW Uroflometry System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801126764. The device is manufactured by APEX MEDITECH from India, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is ENDO INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : B
APEX DIGIFLOW Uroflometry System
Analysis ID: AKL 20801126764

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

APEX MEDITECH

Country of Origin

India

Authorized Representative

ENDO INDONESIA

AR Address

Jl. Raya Menganti 14

Registration Date

Nov 09, 2021

Expiry Date

Dec 31, 2026

Product Type

Diagnostic Gastroenterology-Urology Equipment

Urine flow or volume measuring system.

Non Radiation Electromedics

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