Taiwan FDA registration 18bc1b8bb38f0d7148a23a38586423f4
EMW stethoscope (unsterilized)
TW: EMW聽診器(未滅菌)
Taiwan·Risk Class 1·WUXI KAISHUN MEDICAL APPATUS FACTORY·Registered Oct 30, 2005 – Oct 30, 2015CancelledRegistration details
- Analysis ID
- 18bc1b8bb38f0d7148a23a38586423f4
- Customs Code
- DHA04600003502
Company information
- Manufacturer
- WUXI KAISHUN MEDICAL APPATUS FACTORY
- Manufacturer Country
- China
- Authorized Representative
- Gu Wei Trading Co., Ltd
Product details
- Intended Use
- Manual stethoscope - (1) Identification. A manual stethoscope is a device used to express sounds about the heart, arteries, veins and internal organs.
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.1875 Listening device
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Oct 30, 2005
- Expiry Date
- Oct 30, 2015
- Cancellation Date
- Aug 09, 2018
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for EMW stethoscope (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 18bc1b8bb38f0d7148a23a38586423f4 and manufactured by WUXI KAISHUN MEDICAL APPATUS FACTORY. The authorized representative in Taiwan is Gu Wei Trading Co., Ltd.
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