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"Ito" pressure supply device (unsterilized) - Taiwan Registration 410fe131f40adab9785840fe7ea28a13

Access comprehensive regulatory information for "Ito" pressure supply device (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 410fe131f40adab9785840fe7ea28a13 and manufactured by ITO CO., LTD.. The authorized representative in Taiwan is AMPLE MEDICAL INSTRUMENTS 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.

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410fe131f40adab9785840fe7ea28a13
Registration Details
Taiwan FDA Registration: 410fe131f40adab9785840fe7ea28a13
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Device Details

"Ito" pressure supply device (unsterilized)
TW: "ไผŠ่—ค" ๅฃ“ๅŠ›ไพ›ๆ‡‰่ฃ็ฝฎ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

410fe131f40adab9785840fe7ea28a13

DHA04401100705

Company Information

Japan

Product Details

Limited to the first level of identification scope of "pressure supply devices (O.5765)" under the Measures for the Administration of Medical Devices.

o Physical Medical Sciences

O.5765 ๅฃ“ๅŠ›ไพ›ๆ‡‰่ฃ็ฝฎ

import

Dates and Status

Nov 02, 2011

Nov 02, 2016

Jul 31, 2018

Cancellation Information

Logged out

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