Taiwan FDA registration 27332e7fa8e335ccf47cb41f01016e0a

"Covidien" Sony Xixun bending clamp wireless ultrasonic knife system

TW: “柯惠”索尼西迅彎鉗無線超音波刀系統

Taiwan·Risk Class 2·Covidien llc;; Covidien·Registered May 20, 2019 – May 20, 2029Active

Registration details

Analysis ID: 27332e7fa8e335ccf47cb41f01016e0a
Customs Code: DHA05603254803

Company information

Manufacturer: Covidien llc;; Covidien
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.4400 Cutting and hemostasis electric knives and accessories thereof
Import Information: import

Dates and status

Registration Date: May 20, 2019
Expiry Date: May 20, 2029

About this record

Access comprehensive regulatory information for "Covidien" Sony Xixun bending clamp wireless ultrasonic knife system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 27332e7fa8e335ccf47cb41f01016e0a and manufactured by Covidien llc;; Covidien. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..

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