Taiwan FDA registration 1e51fb4cf96ce0c6221d5ec392427276

"Qiolian" heat and moisture condenser (artificial nose) (unsterilized)

TW: "喬聯" 熱及濕氣凝結器(人工鼻) (未滅菌)

Taiwan·Risk Class 1·Qiaolian Technology Co., Ltd. Nankan Factory·Registered Dec 25, 2013 – Dec 25, 2018Cancelled

Registration details

Analysis ID: 1e51fb4cf96ce0c6221d5ec392427276

Company information

Manufacturer: Qiaolian Technology Co., Ltd. Nankan Factory
Manufacturer Country: Taiwan, Province of China
Authorized Representative: BIOCARE CORPORATION

Product details

Intended Use: Limited to the first level recognition range of the Measures for the Administration of Medical Devices "Heat and Moisture Condenser (Artificial Nose) (D.5375)".
Product Type (Level 1): D Anesthesiology
Product Type (Level 2): D.5375 Heat and humidity condenser (artificial nose)
Import Information: Domestic

Dates and status

Registration Date: Dec 25, 2013
Expiry Date: Dec 25, 2018
Cancellation Date: Jul 15, 2022

Cancellation information

Status: Logged out
Reason: 未展延而逾期者

About this record

Access comprehensive regulatory information for "Qiolian" heat and moisture condenser (artificial nose) (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1e51fb4cf96ce0c6221d5ec392427276 and manufactured by Qiaolian Technology Co., Ltd. Nankan Factory. The authorized representative in Taiwan is BIOCARE CORPORATION.

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