Taiwan FDA registration 2fe1727ea0b6b9480868517bac642dac

"Fantis" decompression cushion (unsterilized)

TW: “芬蒂思”減壓坐墊 (未滅菌)

Taiwan·Risk Class 1·CHENG HOUSE ENTERPRISE CO., LTD.·Registered Apr 27, 2006 – Apr 27, 2011Cancelled

Registration details

Analysis ID: 2fe1727ea0b6b9480868517bac642dac

Company information

Manufacturer: CHENG HOUSE ENTERPRISE CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: FANTASY INDUSTRY CO., LTD.

Product details

Intended Use: It is limited to the first level of identification scope of the "Floating Cushion (O.3175)" of the Administrative Measures for Medical Devices.
Product Type (Level 1): o Physical Medical Sciences
Product Type (Level 2): O.3175 Floating cushion
Import Information: Domestic;; Contract manufacturing

Dates and status

Registration Date: Apr 27, 2006
Expiry Date: Apr 27, 2011
Cancellation Date: Nov 23, 2012

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Fantis" decompression cushion (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2fe1727ea0b6b9480868517bac642dac and manufactured by CHENG HOUSE ENTERPRISE CO., LTD.. The authorized representative in Taiwan is FANTASY INDUSTRY CO., LTD..

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