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"Termao" photography guide set - Taiwan Registration a11f76b475d3d5bca77441b7219eb6f8

Access comprehensive regulatory information for "Termao" photography guide set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a11f76b475d3d5bca77441b7219eb6f8 and manufactured by ASHITAKA FACTORY OF TERUMO CORPORATION. The authorized representative in Taiwan is TERUMO TAIWAN MEDICAL 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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a11f76b475d3d5bca77441b7219eb6f8
Registration Details
Taiwan FDA Registration: a11f76b475d3d5bca77441b7219eb6f8
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Device Details

"Termao" photography guide set
TW: ใ€ๆณฐ็ˆพ่Œ‚ใ€žๆ”ๅฝฑๅผ•ๅฐŽๅฅ—
Risk Class 2

Registration Details

a11f76b475d3d5bca77441b7219eb6f8

DHA00600913400

Company Information

Product Details

E Cardiovascular Medicine Science

E.1340 Catheter Introducers

import

Dates and Status

Apr 27, 1999

Feb 09, 2029