"Termao" single use of guide wire
Taiwan·Risk Class 2·(O) TERUMO CORPORATION;;( P)TERUMO CORPORATION ASHITAKA FACTORY·Registered Mar 28, 2011 – Mar 28, 2026Expired- Analysis ID
- 3740f5388cd8b0947c5c9e31c70c1277
- Customs Code
- DHA00602224502
- Manufacturer Country
- Japan
- Authorized Representative
- YUAN LI INSTRUMENT CO., LTD.
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.1500 Internal Scope and its accessories
- Import Information
- import
- Registration Date
- Mar 28, 2011
- Expiry Date
- Mar 28, 2026
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Access comprehensive regulatory information for "Termao" single use of guide wire in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3740f5388cd8b0947c5c9e31c70c1277 and manufactured by (O) TERUMO CORPORATION;;( P)TERUMO CORPORATION ASHITAKA FACTORY. The authorized representative in Taiwan is YUAN LI INSTRUMENT 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.