"Covidien" V-blade puncture sleeve
Taiwan·Risk Class 2·COVIDIEN LLC;; COVID·Registered May 07, 2013 – May 07, 2018Cancelled- Analysis ID
- d691013a796e392d188be3d7d9fd9c7a
- Customs Code
- DHA00602494906
- Manufacturer
- COVIDIEN LLC;; COVID
- Manufacturer Country
- United States
- Authorized Representative
- Taiwan Covidien Corporation Limited
- 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
- May 07, 2013
- Expiry Date
- May 07, 2018
- Cancellation Date
- Mar 16, 2017
- Status
- Logged out
- Reason
- 公司歇業
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Access comprehensive regulatory information for "Covidien" V-blade puncture sleeve in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d691013a796e392d188be3d7d9fd9c7a and manufactured by COVIDIEN LLC;; COVID. The authorized representative in Taiwan is Taiwan Covidien Corporation Limited.
This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including COVIDIEN LLC;; Covidien, COVIDIEN LLC;; COVID, and 4 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.