Taiwan FDA registration 1e4146c5c037c5a9f4e94e24d4a024be

"Suction Pa" nasal expander (unsterilized)

TW: "吸帕" 鼻腔擴大器 (未滅菌)

Taiwan·Risk Class 1·Shengqing Instrument Factory Co., Ltd·Registered Sep 07, 2016 – Sep 07, 2021Cancelled

Registration details

Analysis ID: 1e4146c5c037c5a9f4e94e24d4a024be

Company information

Manufacturer: Shengqing Instrument Factory Co., Ltd
Manufacturer Country: Taiwan, Province of China
Authorized Representative: Continued Ying Biomedical Co., Ltd

Product details

Intended Use: Limited to the first level recognition range of the "nasal expander (G.3900)" of the Measures for the Administration of Medical Devices.
Product Type (Level 1): G ENT Science
Product Type (Level 2): G.3900 Nasal extenders
Import Information: Domestic;; Contract manufacturing

Dates and status

Registration Date: Sep 07, 2016
Expiry Date: Sep 07, 2021
Cancellation Date: Jun 22, 2022

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Suction Pa" nasal expander (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1e4146c5c037c5a9f4e94e24d4a024be and manufactured by Shengqing Instrument Factory Co., Ltd. The authorized representative in Taiwan is Continued Ying Biomedical Co., Ltd.

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