Taiwan FDA registration 512f8955bb0b929fd302f4ba380d5a72

"Covidien" respirator

TW: “柯惠”呼吸器
Taiwan flagTaiwan·Risk Class 2·COVIDIEN LLC;; Covidien·Registered Dec 31, 2013 – Dec 31, 2023Cancelled
Registration details
Analysis ID
512f8955bb0b929fd302f4ba380d5a72
Customs Code
DHA05602568101
Company information
Manufacturer Country
Ireland;;United States
Authorized Representative
MEDTRONIC (TAIWAN) LTD.
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.5895 Continuous respirators
Import Information
import
Dates and status
Registration Date
Dec 31, 2013
Expiry Date
Dec 31, 2023
Cancellation Date
Sep 21, 2022
Cancellation information
Status
Logged out
Reason
自請註銷
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About this record

Access comprehensive regulatory information for "Covidien" respirator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 512f8955bb0b929fd302f4ba380d5a72 and manufactured by COVIDIEN LLC;; Covidien. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Covidien llc;; Covidien, 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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