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"Termao" sterile adapter - Taiwan Registration 6d58f0cd60176b88c58d5360ed11a404

Access comprehensive regulatory information for "Termao" sterile adapter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6d58f0cd60176b88c58d5360ed11a404 and manufactured by TERUMO CORPORATION;; KOFU FACTORY OF TERUMO CORPORATION. The authorized representative in Taiwan is TERUMO TAIWAN MEDICAL CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including TERUMO CORPORATION;; ASHITAKA FACTORY OF TERUMO CORPORATION, and 1 recent registrations in the same category. 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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6d58f0cd60176b88c58d5360ed11a404
Registration Details
Taiwan FDA Registration: 6d58f0cd60176b88c58d5360ed11a404
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Device Details

"Termao" sterile adapter
TW: "ๆณฐ็ˆพ่Œ‚" ็„ก่ŒๆŽฅๅˆๅ™จ
Risk Class 2
Cancelled

Registration Details

6d58f0cd60176b88c58d5360ed11a404

DHA00601149600

Company Information

Product Details

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

B Hematology, pathology, and genetics

import

Dates and Status

Jun 29, 2005

Jun 29, 2020

Jun 16, 2022

Cancellation Information

Logged out

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