Taiwan FDA registration b275f817e87801756ff7b038cc3282af

"Xinwei" ENT Examination and Treatment Unit (Unsterilized)

TW: “新韋”耳鼻喉檢查及治療檯 (未滅菌)

Taiwan·Risk Class 1·KUANG HSING BIOTECH CO., LTD.·Registered May 01, 2012 – Mar 15, 2022Cancelled

Registration details

Analysis ID: b275f817e87801756ff7b038cc3282af

Company information

Manufacturer: KUANG HSING BIOTECH CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: SHINWEI INSTRUMENT INDUSTRY LTD.

Product details

Intended Use: Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "ENT Examination and Treatment Unit (G.5300)".
Product Type (Level 1): G ENT Science
Product Type (Level 2): G.5300 ENT examination and treatment table
Import Information: Domestic;; Contract manufacturing

Dates and status

Registration Date: May 01, 2012
Expiry Date: Mar 15, 2022
Cancellation Date: Apr 12, 2024

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Xinwei" ENT Examination and Treatment Unit (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b275f817e87801756ff7b038cc3282af and manufactured by KUANG HSING BIOTECH CO., LTD.. The authorized representative in Taiwan is SHINWEI INSTRUMENT INDUSTRY LTD..

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