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EASTTECH Ultrasonic Diagnostic System - Indonesia BPOM Medical Device Registration

EASTTECH Ultrasonic Diagnostic System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501220310. The device is manufactured by DAWEI MEDICAL (JIANGSU) CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. PRIMARY WORKS.

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BPOM Registered
Risk Class Kelas Resiko : B
EASTTECH Ultrasonic Diagnostic System
Analysis ID: AKL 21501220310

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. PRIMARY WORKS

AR Address

Daan Mogot Arcadia Blok F.1/8A-8B Jl. Daan Mogot Km 21, Kelurahan Batu Ceper

Registration Date

Jul 18, 2022

Expiry Date

Jul 17, 2025

Product Type

Diagnostic Radiology Equipment

Ultrasonic pulsed doppler imaging system.

Non Radiation Electromedics

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