Taiwan FDA registration 28060bd45667bb3a24d900703131e9f2

"Baby City" nasal aspirator (unsterilized)

TW: “寶貝城市”吸鼻器 (未滅菌)

Taiwan·Risk Class 1·Xuqiao Rubber Enterprise Co., Ltd·Registered Jul 27, 2010 – Jul 27, 2015Cancelled

Registration details

Analysis ID: 28060bd45667bb3a24d900703131e9f2

Company information

Manufacturer: Xuqiao Rubber Enterprise Co., Ltd
Manufacturer Country: Taiwan, Province of China
Authorized Representative: BUDURB CO., LTD.

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Lavage Syringe (J.6960)".
Product Type (Level 1): J General hospital and personal use equipment
Product Type (Level 2): J.6960 Lavage syringe
Import Information: Domestic;; Contract manufacturing

Dates and status

Registration Date: Jul 27, 2010
Expiry Date: Jul 27, 2015
Cancellation Date: Jun 26, 2018

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Baby City" nasal aspirator (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 28060bd45667bb3a24d900703131e9f2 and manufactured by Xuqiao Rubber Enterprise Co., Ltd. The authorized representative in Taiwan is BUDURB CO., LTD..

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