Taiwan FDA registration f64ec6dadcad1f25f42e0c51d103e0cc
"Covidien" Merlin Cosa Tongshi Inner Tracheal Probe (Unsterilized)
TW: "柯惠"麥林可莎彤史利氣管內管探針 (未滅菌)
Taiwan·Risk Class 1·COVIDIEN LLC;; MALLINCKRODT MEDICAL·Registered May 23, 2006 – May 23, 2021CancelledRegistration details
- Analysis ID
- f64ec6dadcad1f25f42e0c51d103e0cc
- Customs Code
- DHA04400457002
Company information
- Manufacturer
- COVIDIEN LLC;; MALLINCKRODT MEDICAL
- Manufacturer Country
- Ireland;;United States
- Authorized Representative
- Taiwan Covidien Corporation Limited
Product details
- Intended Use
- Limited to the first level recognition range of endotracheal tube probe (D.5790) of the management method for medical equipment.
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5790 氣管內管探針
- Import Information
- import
Dates and status
- Registration Date
- May 23, 2006
- Expiry Date
- May 23, 2021
- Cancellation Date
- Mar 16, 2017
Cancellation information
- Status
- Logged out
- Reason
- 公司歇業
About this record
Access comprehensive regulatory information for "Covidien" Merlin Cosa Tongshi Inner Tracheal Probe (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f64ec6dadcad1f25f42e0c51d103e0cc and manufactured by COVIDIEN LLC;; MALLINCKRODT MEDICAL. The authorized representative in Taiwan is Taiwan Covidien Corporation Limited.
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.
Free DatabasePowered by Pure Global AI89,000+ Devices