Taiwan FDA registration 98b17b99d3cd2b2f5fdcb819443a3554
Xingjie Nose Cleanse Physiological Seawater Sprayer (Unsterilized)
TW: 星捷舒鼻淨 生理海水噴霧器 (未滅菌)
Registration details
- Analysis ID
- 98b17b99d3cd2b2f5fdcb819443a3554
- Customs Code
- DHA04401250500
Company information
- Manufacturer
- KOIKE CHEMICAL CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- Guangxin Pharmaceutical Co., Ltd
Product details
- Intended Use
- Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "ENT Dispensing Devices (G.5220)".
- Product Type (Level 1)
- G ENT Science
- Product Type (Level 2)
- G.5220 Ear, nose and throat applicators and substances used in conjunction thereof
- Import Information
- import
Dates and status
- Registration Date
- Dec 19, 2012
- Expiry Date
- Dec 19, 2017
- Cancellation Date
- Nov 28, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Xingjie Nose Cleanse Physiological Seawater Sprayer (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 98b17b99d3cd2b2f5fdcb819443a3554 and manufactured by KOIKE CHEMICAL CO., LTD.. The authorized representative in Taiwan is Guangxin Pharmaceutical Co., Ltd.
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices