Taiwan FDA registration ef9077aeed2fc0673f81ab2dff7b353f
"Riester" Manual Stethoscope (Non-Sterile)
TW: "瑞司" 手動聽診器 (未滅菌)
Taiwan·Risk Class 1·MD·Rudolf Riester GmbH·Registered Jul 11, 2016 – Jul 11, 2026ExpiredRegistration details
- Analysis ID
- ef9077aeed2fc0673f81ab2dff7b353f
- License Form
- Ministry of Health Medical Device Import No. 016761
- Customs Code
- DHA09401676105
Company information
- Manufacturer
- Rudolf Riester GmbH
- Manufacturer Country
- Germany
- Authorized Representative
- BOYANG MEDICAL TECHNOLOGY CO., LTD
Product details
- Intended Use
- Limited to the first-level identification range of the "stethoscope (E.1875)" of the Measures for the Administration of Medical Equipment.
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E1875 stethoscope
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 11, 2016
- Expiry Date
- Jul 11, 2026
About this record
Access comprehensive regulatory information for "Riester" Manual Stethoscope (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ef9077aeed2fc0673f81ab2dff7b353f and manufactured by Rudolf Riester GmbH. The authorized representative in Taiwan is BOYANG MEDICAL TECHNOLOGY 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