Taiwan FDA registration b5b92ad9684416e9f7b6f4a352c336a1

"Covidien" non-absorbable wound suture device

TW: “柯惠”不可吸收傷口縫合裝置

Taiwan·Risk Class 2·COVIDIEN LLC;; COVID·Registered May 25, 2015 – May 25, 2030Active

Registration details

Analysis ID: b5b92ad9684416e9f7b6f4a352c336a1
Customs Code: DHA05602739408

Company information

Manufacturer: COVIDIEN LLC;; COVID
Manufacturer Country: 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): I General, Plastic Surgery and Dermatology
Product Type (Level 2): I.5000 Non-absorbable polyethylene terephthalate sewing wire
Import Information: import

Dates and status

Registration Date: May 25, 2015
Expiry Date: May 25, 2030

About this record

Access comprehensive regulatory information for "Covidien" non-absorbable wound suture device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b5b92ad9684416e9f7b6f4a352c336a1 and manufactured by COVIDIEN LLC;; COVID. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..

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