Taiwan FDA registration e8dda693a94196a0b521c309c032db93

"Medtronic" Aseanda implantable spinal cord endoluminal catheter

TW: “美敦力”亞善達植入式脊髓腔內導管

Taiwan·Risk Class 3·Medtronic Puerto Rico Operations Co., Juncos;; Medtronic Inc.·Registered May 02, 2019 – May 02, 2029Active

Registration details

Analysis ID: e8dda693a94196a0b521c309c032db93
Customs Code: DHA05603259104

Company information

Manufacturer: Medtronic Puerto Rico Operations Co., Juncos;; Medtronic Inc.
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): J General hospital and personal use equipment
Product Type (Level 2): J.9999 Miscellaneous
Import Information: import

Dates and status

Registration Date: May 02, 2019
Expiry Date: May 02, 2029

About this record

Access comprehensive regulatory information for "Medtronic" Aseanda implantable spinal cord endoluminal catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number e8dda693a94196a0b521c309c032db93 and manufactured by Medtronic Puerto Rico Operations Co., Juncos;; Medtronic Inc.. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..

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