Taiwan FDA registration 1d4453acde18f9990d23e109a7507ba4

"Xingang" respirator

TW: "新港"呼吸器
Taiwan flagTaiwan·Risk Class 2·COVIDIEN LLC;; Covidien·Registered Sep 18, 1996 – Feb 09, 2019Cancelled
Registration details
Analysis ID
1d4453acde18f9990d23e109a7507ba4
Customs Code
DHA00600800408
Company information
Manufacturer Country
Ireland;;United States
Authorized Representative
MEDTRONIC (TAIWAN) LTD.
Product details
Product Type (Level 1)
0200 Respiratory Assist
Import Information
Contract manufacturing;; input
Dates and status
Registration Date
Sep 18, 1996
Expiry Date
Feb 09, 2019
Cancellation Date
Jun 16, 2022
Cancellation information
Status
Logged out
Reason
自行鍵入
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About this record

Access comprehensive regulatory information for "Xingang" respirator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1d4453acde18f9990d23e109a7507ba4 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 3 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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