Taiwan FDA registration 8dbd4bc43a4226e10933ff0095adc449

"Huaxi" laryngeal flash endoscope (unsterilized)

TW: "華陞" 喉頭閃頻內視鏡 (未滅菌)

Taiwan·Risk Class 1·HUA SHENG INSTRUMENTS CO., LTD.·Registered Dec 09, 2011 – Dec 09, 2016Cancelled

Registration details

Analysis ID: 8dbd4bc43a4226e10933ff0095adc449

Company information

Manufacturer: HUA SHENG INSTRUMENTS CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: HUA SHENG INSTRUMENTS CO., LTD.

Product details

Intended Use: Limited to the first level identification range of the Measures for the Administration of Medical Devices "Laryngeal Flash Endoscopy (G.4750)".
Product Type (Level 1): G ENT Science
Product Type (Level 2): G.4750 Throat frequented internal mirrors
Import Information: Domestic

Dates and status

Registration Date: Dec 09, 2011
Expiry Date: Dec 09, 2016
Cancellation Date: May 25, 2018

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Huaxi" laryngeal flash endoscope (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 8dbd4bc43a4226e10933ff0095adc449 and manufactured by HUA SHENG INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is HUA SHENG INSTRUMENTS CO., LTD..

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