Pure Global

"Arkard" ophthalmic ultrasound scanner - Taiwan Registration a5d9081baf5d4991dd19090380ceb3ce

Access comprehensive regulatory information for "Arkard" ophthalmic ultrasound scanner in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a5d9081baf5d4991dd19090380ceb3ce and manufactured by ACCUTOME, INC.. The authorized representative in Taiwan is BIOMEGA INSTRUMENT CO., LTD..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

Free Database
Powered by Pure Global AI
89,000+ Devices
a5d9081baf5d4991dd19090380ceb3ce
Registration Details
Taiwan FDA Registration: a5d9081baf5d4991dd19090380ceb3ce
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Arkard" ophthalmic ultrasound scanner
TW: โ€œๆ„›ๅฏๅพทโ€็œผ็ง‘่ถ…้ŸณๆณขๆŽƒๆๅ„€
Risk Class 2
Cancelled

Registration Details

a5d9081baf5d4991dd19090380ceb3ce

DHA05602774409

Company Information

United States

Product Details

For details, it is Chinese approved copy of the imitation order

P Radiology Science

P.1560 Ultrasonic Echo Imaging System;; P.1570 Ultrasonic converters for diagnostic use

import

Dates and Status

Sep 30, 2015

Sep 30, 2020

Jun 16, 2022

Cancellation Information

Logged out

่‡ช่กŒ้ตๅ…ฅ