Taiwan FDA registration 876443cc42192a1db21edcc0b18136b6

"Medtronic" spinal endoluminal catheter

TW: “美敦力” 脊髓腔內導管

Taiwan·Risk Class 3·Medtronic Puerto Rico Operations Co., Juncos;; Medtronic Inc.·Registered Nov 04, 2013 – Nov 04, 2023Expired

Registration details

Analysis ID: 876443cc42192a1db21edcc0b18136b6
Customs Code: DHA05602557301

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: Nov 04, 2013
Expiry Date: Nov 04, 2023

About this record

Access comprehensive regulatory information for "Medtronic" spinal 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 876443cc42192a1db21edcc0b18136b6 and manufactured by Medtronic Puerto Rico Operations Co., Juncos;; Medtronic Inc.. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..

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