Taiwan FDA registration 34a388b8a1150d13d9e6c3f3c7e02af5

Medtronic ENT Manual Surgical Instruments (Unsterilized)

TW: “美敦力”耳鼻喉手動式外科器械 (未滅菌)

Taiwan·Risk Class 1·MEDTRONIC XOMED INSTRUMENTATION SAS·Registered Jan 14, 2010 – Jan 14, 2020Cancelled

Registration details

Analysis ID: 34a388b8a1150d13d9e6c3f3c7e02af5
Customs Code: DHA04400846206

Company information

Manufacturer: MEDTRONIC XOMED INSTRUMENTATION SAS
Manufacturer Country: France
Authorized Representative: MEDTRONIC (TAIWAN) LTD.

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Devices "ENT Manual Surgical Instruments (G.4420)".
Product Type (Level 1): G ENT Science
Product Type (Level 2): G.4420 Otolaryngology manual surgical instruments
Import Information: import

Dates and status

Registration Date: Jan 14, 2010
Expiry Date: Jan 14, 2020
Cancellation Date: Jun 16, 2022

Cancellation information

Status: Logged out
Reason: 自行鍵入

About this record

Access comprehensive regulatory information for Medtronic ENT Manual Surgical Instruments (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 34a388b8a1150d13d9e6c3f3c7e02af5 and manufactured by MEDTRONIC XOMED INSTRUMENTATION SAS. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..

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