Taiwan FDA registration e668253b1d96c6bd4744deb5827492f8

"Covidien" Vivienco Sherry Extended Pneumatic Cannula

TW: “柯惠”萬靈科雪莉加長型氣切套管
Taiwan flagTaiwan·Risk Class 2·COVIDIEN LLC;; MALLINCKRODT MEDICAL·Registered Dec 27, 2013 – Dec 27, 2018Cancelled
Registration details
Analysis ID
e668253b1d96c6bd4744deb5827492f8
Customs Code
DHA05602567901
Company information
Manufacturer Country
Ireland;;United States
Authorized Representative
Taiwan Covidien Corporation Limited
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
D Anesthesiology
Product Type (Level 2)
D.5800 氣切管及其氣囊
Import Information
import
Dates and status
Registration Date
Dec 27, 2013
Expiry Date
Dec 27, 2018
Cancellation Date
Mar 16, 2017
Cancellation information
Status
Logged out
Reason
公司歇業
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About this record

Access comprehensive regulatory information for "Covidien" Vivienco Sherry Extended Pneumatic Cannula in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e668253b1d96c6bd4744deb5827492f8 and manufactured by COVIDIEN LLC;; MALLINCKRODT MEDICAL. The authorized representative in Taiwan is Taiwan Covidien Corporation Limited.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including COVIDIEN LLC;; MALLINCKRODT MEDICAL, 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.

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