"Covidien" V-blade puncture sleeve - Taiwan Registration 00ecb4df9e684f02bdd1b4c1164cf767
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 00ecb4df9e684f02bdd1b4c1164cf767 and manufactured by COVIDIEN LLC;; Covidien. 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
Registration Details
00ecb4df9e684f02bdd1b4c1164cf767
DHA00601365109
Product Details
For details, it is Chinese approved copy of the imitation order
H Gastroenterology and urology
import
Dates and Status
Nov 23, 2005
Nov 23, 2020
Jun 16, 2022
Cancellation Information
Logged out
่ช่ก้ตๅ ฅ
"Covidien" V-blade puncture sleeve
COVIDIEN LLC;; COVID
d691013a796e392d188be3d7d9fd9c7a
2
"Covidien" V-blade puncture sleeve
COVIDIEN LLC;; COVID
acc2f54fa27bbf0350a5f30208f99f3d
2
"Covidien" V-blade puncture sleeve
COVIDIEN LLC;; Covidien
53fc11d7c23d2892b7fc7e4c9a486c76
2
"Covidien" V-blade puncture sleeve
COVIDIEN LLC;; Covidien
c5a1921757605055fc6d84355ddb63b6
2

