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"Pomedon" abruptly plastic artificial - Taiwan Registration 59574022f382f385c8330c1ad0b6dbaa

Access comprehensive regulatory information for "Pomedon" abruptly plastic artificial in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 59574022f382f385c8330c1ad0b6dbaa and manufactured by Promedon S.A.. The authorized representative in Taiwan is Foresee Medical 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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59574022f382f385c8330c1ad0b6dbaa
Registration Details
Taiwan FDA Registration: 59574022f382f385c8330c1ad0b6dbaa
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Device Details

"Pomedon" abruptly plastic artificial
TW: โ€œๅš็พŽๆ•ฆโ€็ชๅ‹ƒๅฏๅก‘ๆ€งไบบๅทฅ้™ฐ่Ž–
Risk Class 2

Registration Details

59574022f382f385c8330c1ad0b6dbaa

DHA05602676703

Company Information

Argentina

Product Details

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

H Gastroenterology and urology

H.3630 ็กฌๅผ้™ฐ่Ž–ๆคๅ…ฅ็‰ฉ

import

Dates and Status

Oct 31, 2014

Oct 31, 2029