Taiwan FDA registration 228d4960907a228a84900d9d0382c4dd

"Uni" sputum tube (unsterilized)

TW: "宇仁" 抽痰管 (未滅菌)

Taiwan·Risk Class 1·INNOVATIVE MEDICAL MANUFACTURING COMPANY·Registered Mar 06, 2015 – Mar 06, 2020Cancelled

Registration details

Analysis ID: 228d4960907a228a84900d9d0382c4dd

Company information

Manufacturer: INNOVATIVE MEDICAL MANUFACTURING COMPANY
Manufacturer Country: Taiwan, Province of China
Authorized Representative: INNOVATIVE MEDICAL MANUFACTURING COMPANY

Product details

Intended Use: Limited to the management method of medical equipment, tracheobronchial suction catheter (D.6810) level 1 identification range.
Product Type (Level 1): D Anesthesiology
Product Type (Level 2): D.6810 Pneumatic bronchial suction guide tube
Import Information: Domestic

Dates and status

Registration Date: Mar 06, 2015
Expiry Date: Mar 06, 2020
Cancellation Date: Jun 16, 2022

Cancellation information

Status: Logged out
Reason: 自行鍵入

About this record

Access comprehensive regulatory information for "Uni" sputum tube (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 228d4960907a228a84900d9d0382c4dd and manufactured by INNOVATIVE MEDICAL MANUFACTURING COMPANY. The authorized representative in Taiwan is INNOVATIVE MEDICAL MANUFACTURING COMPANY.

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