Taiwan FDA registration 825abcf3360fe410f13805196722e3bb
"Besmed" Silicone VESSEL LOOPS (Non-Sterile)
TW: "貝斯美德" 矽質血管識別帶(未滅菌)
Taiwan·Risk Class 1·MD·BESMED HEALTH BUSINESS CORP.·Registered Mar 16, 2020 – Mar 16, 2025ExpiredRegistration details
- Analysis ID
- 825abcf3360fe410f13805196722e3bb
- License Form
- Ministry of Health Medical Device Manufacturing No. 008235
Company information
- Manufacturer
- BESMED HEALTH BUSINESS CORP.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- BESMED HEALTH BUSINESS CORP.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I4800 General Surgery Manual Instrument
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Mar 16, 2020
- Expiry Date
- Mar 16, 2025
About this record
Access comprehensive regulatory information for "Besmed" Silicone VESSEL LOOPS (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 825abcf3360fe410f13805196722e3bb and manufactured by BESMED HEALTH BUSINESS CORP.. The authorized representative in Taiwan is BESMED HEALTH BUSINESS CORP..
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