Taiwan FDA registration 82512eea30bdadb2a4b734adffea3cf8
"Perth" Instruments for Cardiac Surgery (Unsterilized)
TW: "伯斯" 心臟外科手術用器械 (未滅菌)
Taiwan·Risk Class 1·BOSS INSTRUMENTS, INC.·Registered Apr 13, 2006 – Apr 13, 2011CancelledRegistration details
- Analysis ID
- 82512eea30bdadb2a4b734adffea3cf8
- Customs Code
- DHA04400373006
Company information
- Manufacturer
- BOSS INSTRUMENTS, INC.
- Manufacturer Country
- United States
- Authorized Representative
- Shake Universe Enterprises Limited
Product details
- Intended Use
- It is limited to the scope of first-level identification of medical devices management measures (cardiovascular surgical devices [E.4500]).
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.4500 心臟血管外科器械
- Import Information
- import
Dates and status
- Registration Date
- Apr 13, 2006
- Expiry Date
- Apr 13, 2011
- Cancellation Date
- Nov 16, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Perth" Instruments for Cardiac Surgery (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 82512eea30bdadb2a4b734adffea3cf8 and manufactured by BOSS INSTRUMENTS, INC.. The authorized representative in Taiwan is Shake Universe Enterprises Limited.
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