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"Termao" sterile adapter - Taiwan Registration a4b5a4d412e2814c43a977e00eecb1cf

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 a4b5a4d412e2814c43a977e00eecb1cf 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, 1 companies making similar products including TERUMO CORPORATION;; KOFU 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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a4b5a4d412e2814c43a977e00eecb1cf
Registration Details
Taiwan FDA Registration: a4b5a4d412e2814c43a977e00eecb1cf
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Device Details

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

Registration Details

a4b5a4d412e2814c43a977e00eecb1cf

DHA00601715007

Company Information

Product Details

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

B Hematology, pathology, and genetics

B.9875 Shift set

import

Dates and Status

Sep 26, 2006

Sep 26, 2026

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