Taiwan FDA registration e42f300e4dc07e0dd70a0de82e6e57fe

"Medtronic" Non-powered Neurosurgical Instruments (Sterilized)

TW: "美敦力" 非動力式神經外科手術器械 (滅菌)

Taiwan·Risk Class 1·Medtronic Puerto Rico Operations Co., Juncos;; Medtronic Inc.·Registered Dec 25, 2018 – Dec 25, 2028Active

Registration details

Analysis ID: e42f300e4dc07e0dd70a0de82e6e57fe
Customs Code: DHA09401995800

Company information

Manufacturer: Medtronic Puerto Rico Operations Co., Juncos;; Medtronic Inc.
Manufacturer Country: United States
Authorized Representative: MEDTRONIC (TAIWAN) LTD.

Product details

Intended Use: It is limited to the first level of identification scope of the "Non-powered Neurosurgical Devices (K.4535)" of the Measures for the Classification and Grading of Medical Devices.
Product Type (Level 1): K Neuroscience
Product Type (Level 2): K.4535 非動力式神經外科用器械
Import Information: Input;; QMS/QSD

Dates and status

Registration Date: Dec 25, 2018
Expiry Date: Dec 25, 2028

About this record

Access comprehensive regulatory information for "Medtronic" Non-powered Neurosurgical Instruments (Sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e42f300e4dc07e0dd70a0de82e6e57fe and manufactured by Medtronic Puerto Rico Operations Co., Juncos;; Medtronic Inc.. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..

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