Taiwan FDA registration 0b19ed7c84e3bdbd8a38b35d1dec8ddb
Velen stethoscope (unsterilized)
TW: 〝韋倫〞聽診器(未滅菌)
Taiwan·Risk Class 1·WELCH ALLYN INC.·Registered Nov 15, 2005 – Nov 15, 2020CancelledRegistration details
- Analysis ID
- 0b19ed7c84e3bdbd8a38b35d1dec8ddb
- Customs Code
- DHA04400194800
Company information
- Manufacturer
- WELCH ALLYN INC.
- Manufacturer Country
- United States
- Authorized Representative
- JAG MEDICAL CO., LTD.
Product details
- Intended Use
- 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
- import
Dates and status
- Registration Date
- Nov 15, 2005
- Expiry Date
- Nov 15, 2020
- Cancellation Date
- Jun 07, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Velen 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 0b19ed7c84e3bdbd8a38b35d1dec8ddb and manufactured by WELCH ALLYN INC.. The authorized representative in Taiwan is JAG MEDICAL CO., LTD..
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