Taiwan FDA registration 99922fc2ccfe251cf4f0c5e7bc0f0042

"Medtronic" Aitan superior magnetic resonance contrast electrode leads

TW: “美敦力”艾坦卓越磁振造影電極導線

Taiwan·Risk Class 3·Medtronic Inc.;; MEDTRONIC PUERTO RICO OPERATIONS CO., VILLALBA·Registered Jun 30, 2017 – Jun 30, 2027Active

Registration details

Analysis ID: 99922fc2ccfe251cf4f0c5e7bc0f0042
Customs Code: DHA05602995200

Company information

Manufacturer: Medtronic Inc.;; MEDTRONIC PUERTO RICO OPERATIONS CO., VILLALBA
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): E Cardiovascular Medicine Science
Product Type (Level 2): E.3680 心血管用永久或暫時性之心律調節器電極
Import Information: import

Dates and status

Registration Date: Jun 30, 2017
Expiry Date: Jun 30, 2027

About this record

Access comprehensive regulatory information for "Medtronic" Aitan superior magnetic resonance contrast electrode leads in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 99922fc2ccfe251cf4f0c5e7bc0f0042 and manufactured by Medtronic Inc.;; MEDTRONIC PUERTO RICO OPERATIONS CO., VILLALBA. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..

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