Taiwan FDA registration 00dc6d82082513ad50f69a144d737b85

"Medtronic" McGrath Rigid Laryngoscope (Sterilized)

TW: "美敦力" 麦格拉斯硬式喉頭鏡 (滅菌)

Taiwan·Risk Class 1·COVIDIEN LLC;; Xubang Medical Equipment Co., Ltd·Registered May 04, 2017 – May 04, 2027Active

Registration details

Analysis ID: 00dc6d82082513ad50f69a144d737b85

Company information

Manufacturer: COVIDIEN LLC;; Xubang Medical Equipment Co., Ltd
Manufacturer Country: Taiwan, Province of China;;United States
Authorized Representative: MEDTRONIC (TAIWAN) LTD.

Product details

Intended Use: Limited to the first level identification range of the "rigid laryngoscope (D.5540)" of the Measures for the Classification and Grading Management of Medical Devices.
Product Type (Level 1): D Anesthesiology
Product Type (Level 2): D.5540 Rigid laryngoscope
Import Information: 國產;; 委託製造;; QMS/QSD

Dates and status

Registration Date: May 04, 2017
Expiry Date: May 04, 2027

About this record

Access comprehensive regulatory information for "Medtronic" McGrath Rigid Laryngoscope (Sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 00dc6d82082513ad50f69a144d737b85 and manufactured by COVIDIEN LLC;; Xubang Medical Equipment Co., Ltd. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..

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