"Termao" sterile adapter
Taiwan·Risk Class 2·TERUMO CORPORATION;; ASHITAKA FACTORY OF TERUMO CORPORATION·Registered Sep 26, 2006 – Sep 26, 2026Active- Analysis ID
- a4b5a4d412e2814c43a977e00eecb1cf
- Customs Code
- DHA00601715007
- Manufacturer Country
- Japan
- Authorized Representative
- TERUMO TAIWAN MEDICAL CO., LTD.
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.9875 Shift set
- Import Information
- import
- Registration Date
- Sep 26, 2006
- Expiry Date
- Sep 26, 2026
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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.