Taiwan FDA registration 06b90ac8645d4d1a9d1ce6fd32a23cfb
"Medtronic" Cyon endoscope sheath system
TW: “美敦力”賽昂內視鏡鞘管系統
Registration details
- Analysis ID
- 06b90ac8645d4d1a9d1ce6fd32a23cfb
- Customs Code
- DHA00602010907
Company information
- Manufacturer Country
- Dominican Republic;;United States
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- G ENT Science
- Product Type (Level 2)
- G.4760 Nasopharyngeal scopes (soft or rigid) and their accessories
- Import Information
- import
Dates and status
- Registration Date
- Aug 12, 2009
- Expiry Date
- Aug 12, 2029
About this record
Access comprehensive regulatory information for "Medtronic" Cyon endoscope sheath system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 06b90ac8645d4d1a9d1ce6fd32a23cfb and manufactured by MEDTRONIC XOMED, INC;; Made (部分製程) in DOMINICAN REPUBLIC. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) 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