Taiwan FDA registration 5fb1c555b2696001ae763b58006b4a27

"Covidien" L-connector (double helix interface) (sterilization)

TW: ”柯惠”L型連接頭(雙螺旋接口)(滅菌)

Taiwan·Risk Class 1·COVIDIEN LLC;; MALLINCKRODT MEDICAL·Registered Jan 23, 2006 – Jan 23, 2026Expired

Registration details

Analysis ID: 5fb1c555b2696001ae763b58006b4a27
Customs Code: DHA04400255305

Company information

Manufacturer: COVIDIEN LLC;; MALLINCKRODT MEDICAL
Manufacturer Country: Ireland;;United States
Authorized Representative: MEDTRONIC (TAIWAN) LTD.

Product details

Intended Use: An airway connector is a device that connects breathing gas to an endotracheal tube, tracheostomy tube, or mask.
Product Type (Level 1): D Anesthesiology
Product Type (Level 2): D.5810 Airway connectors
Import Information: import

Dates and status

Registration Date: Jan 23, 2006
Expiry Date: Jan 23, 2026

About this record

Access comprehensive regulatory information for "Covidien" L-connector (double helix interface) (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5fb1c555b2696001ae763b58006b4a27 and manufactured by COVIDIEN LLC;; MALLINCKRODT MEDICAL. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..

This page provides complete technical specifications, regulatory compliance details. 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.