Taiwan FDA registration d6c246235dd77207019c19c0fea5351b

"Covidien" Neput respirator

TW: "柯惠"奈普特呼吸器
Taiwan flagTaiwan·Risk Class 2·COVIDIEN LLC;; Covidien·Registered Jul 11, 2001 – Jul 11, 2021Cancelled
Registration details
Analysis ID
d6c246235dd77207019c19c0fea5351b
Customs Code
DHA00600969807
Company information
Manufacturer Country
Ireland;;United States
Authorized Representative
MEDTRONIC (TAIWAN) LTD.
Product details
Product Type (Level 1)
D000 Anesthesiology
Import Information
Input;; Contract manufacturing
Dates and status
Registration Date
Jul 11, 2001
Expiry Date
Jul 11, 2021
Cancellation Date
Oct 12, 2023
Cancellation information
Status
Logged out
Reason
未展延而逾期者
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About this record

Access comprehensive regulatory information for "Covidien" Neput respirator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d6c246235dd77207019c19c0fea5351b and manufactured by COVIDIEN LLC;; Covidien. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..

This page provides complete technical specifications, regulatory compliance details, 3 companies making similar products including COVIDIEN LLC;; Covidien, Covidien llc;; Covidien, 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.

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