Taiwan FDA registration fe3a125a16a7070e86551132b42d1fb8

"Ward" breathing mouthpiece (unsterilized)

TW: "華德" 呼吸咬嘴 (未滅菌)

Taiwan·Risk Class 1·HEADSTAR MEDICAL PRODUCTS CO., LTD.·Registered Oct 28, 2016 – Oct 28, 2021Cancelled

Registration details

Analysis ID: fe3a125a16a7070e86551132b42d1fb8

Company information

Manufacturer: HEADSTAR MEDICAL PRODUCTS CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: HEADSTAR MEDICAL PRODUCTS CO., LTD.

Product details

Intended Use: Limited to the first level identification range of the Measures for the Administration of Medical Devices "Respiratory Bites (D.5620)".
Product Type (Level 1): D Anesthesiology
Product Type (Level 2): D.5620 Breathing mouthpiece
Import Information: Domestic

Dates and status

Registration Date: Oct 28, 2016
Expiry Date: Oct 28, 2021
Cancellation Date: Aug 15, 2023

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Ward" breathing mouthpiece (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number fe3a125a16a7070e86551132b42d1fb8 and manufactured by HEADSTAR MEDICAL PRODUCTS CO., LTD.. The authorized representative in Taiwan is HEADSTAR MEDICAL PRODUCTS CO., LTD..

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