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"Termo" Navoklos supports the catheter - Taiwan Registration d2c01c4caf20c930e32c399edcd283ad

Access comprehensive regulatory information for "Termo" Navoklos supports the catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d2c01c4caf20c930e32c399edcd283ad and manufactured by TERUMO CORPORATION;; 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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d2c01c4caf20c930e32c399edcd283ad
Registration Details
Taiwan FDA Registration: d2c01c4caf20c930e32c399edcd283ad
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Device Details

"Termo" Navoklos supports the catheter
TW: โ€œๆณฐ็ˆพ่Œ‚โ€็ดไผๅ…‹ๆด›ๆ–ฏๆ”ฏๆŒๅฐŽ็ฎก
Risk Class 2

Registration Details

d2c01c4caf20c930e32c399edcd283ad

DHA05602967309

Company Information

Product Details

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

E Cardiovascular Medicine Science

E.1250 Percutaneous catheters

import

Dates and Status

Apr 21, 2017

Apr 21, 2027