Taiwan FDA registration 8a30fe27cc70d94847bb36aa2301d60d

"Covidien" respirator

TW: “柯惠”呼吸器
Taiwan flagTaiwan·Risk Class 2·Covidien llc;; Covidien·Registered May 24, 2012 – May 24, 2022Cancelled
Registration details
Analysis ID
8a30fe27cc70d94847bb36aa2301d60d
Customs Code
DHA00602351201
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
May 24, 2012
Expiry Date
May 24, 2022
Cancellation Date
Apr 12, 2024
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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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 8a30fe27cc70d94847bb36aa2301d60d 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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