"Covidien" V-blade puncture sleeve - Taiwan Registration acc2f54fa27bbf0350a5f30208f99f3d
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 acc2f54fa27bbf0350a5f30208f99f3d and manufactured by COVIDIEN LLC;; COVID. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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.
Device Details
Product Details
For details, it is Chinese approved copy of the imitation order
H Gastroenterology and urology
H.1500 Internal Scope and its accessories
import
Dates and Status
Apr 30, 2013
Apr 30, 2018
Dec 13, 2019
Cancellation Information
Logged out
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"Covidien" V-blade puncture sleeve
COVIDIEN LLC;; COVID
d691013a796e392d188be3d7d9fd9c7a
2
"Covidien" V-blade puncture sleeve
COVIDIEN LLC;; Covidien
53fc11d7c23d2892b7fc7e4c9a486c76
2
"Covidien" V-blade puncture sleeve
COVIDIEN LLC;; Covidien
00ecb4df9e684f02bdd1b4c1164cf767
2
"Covidien" V-blade puncture sleeve
COVIDIEN LLC;; Covidien
c5a1921757605055fc6d84355ddb63b6
2