Taiwan FDA registration 14402dac7af4afcdb22ae01b461e2e21
"Kaini" nasal aspirator (unsterilized)
TW: “貝印”吸鼻器 (未滅菌)
Taiwan·Risk Class 1·KAI INDUSTRIES CO., LTD.·Registered Apr 06, 2009 – Apr 06, 2014CancelledRegistration details
- Analysis ID
- 14402dac7af4afcdb22ae01b461e2e21
- Customs Code
- DHA04400762200
Company information
- Manufacturer
- KAI INDUSTRIES CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- Jintai Industrial 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
- import
Dates and status
- Registration Date
- Apr 06, 2009
- Expiry Date
- Apr 06, 2014
- Cancellation Date
- Jan 09, 2017
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Kaini" 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 14402dac7af4afcdb22ae01b461e2e21 and manufactured by KAI INDUSTRIES CO., LTD.. The authorized representative in Taiwan is Jintai Industrial Co., Ltd.
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