Taiwan FDA registration 29f2251758c4d59a6e913e8fc32f8e01
"Ames" stethoscope (unsterilized)
TW: "愛美士" 聽診器 (未滅菌)
Taiwan·Risk Class 1·S. MES. CO., LTD.·Registered Jan 03, 2006 – Jan 03, 2016CancelledRegistration details
- Analysis ID
- 29f2251758c4d59a6e913e8fc32f8e01
- Customs Code
- DHY04300091502
Company information
- Manufacturer
- S. MES. CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- S. MES. 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
- Domestic
Dates and status
- Registration Date
- Jan 03, 2006
- Expiry Date
- Jan 03, 2016
- Cancellation Date
- Jun 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Ames" 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 29f2251758c4d59a6e913e8fc32f8e01 and manufactured by S. MES. CO., LTD.. The authorized representative in Taiwan is S. MES. 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