Taiwan FDA registration cd03151020c7fc720f27e2dbed112e59
"Whirlton" air conduction hearing aids (unsterilized)
TW: “ 惠耳通 ”氣導助聽器 (未滅菌)
Taiwan·Risk Class 1·VIVATONE HEARING SYSTEMS, LLC·Registered Apr 27, 2006 – Apr 27, 2011CancelledRegistration details
- Analysis ID
- cd03151020c7fc720f27e2dbed112e59
- Customs Code
- DHA04400425701
Company information
- Manufacturer
- VIVATONE HEARING SYSTEMS, LLC
- Manufacturer Country
- United States
- Authorized Representative
- TEAM-BEST INC.
Product details
- Intended Use
- Limited medical equipment management method "Hearing Aid (G.3300)" first-class classification scope.
- Product Type (Level 1)
- G ENT Science
- Product Type (Level 2)
- G.3300 Hearing Aids
- Import Information
- import
Dates and status
- Registration Date
- Apr 27, 2006
- Expiry Date
- Apr 27, 2011
- Cancellation Date
- Dec 16, 2010
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Whirlton" air conduction hearing aids (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number cd03151020c7fc720f27e2dbed112e59 and manufactured by VIVATONE HEARING SYSTEMS, LLC. The authorized representative in Taiwan is TEAM-BEST INC..
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