Taiwan FDA registration 05dec9f51beb42524754bc042db823e0
"Thunderbolt" aortic punch (unsterilized)
TW: "霹霖" 主動脈打孔器 (未滅菌)
Taiwan·Risk Class 1·PILLING SURGICAL·Registered Feb 07, 2006 – Feb 07, 2011CancelledRegistration details
- Analysis ID
- 05dec9f51beb42524754bc042db823e0
- Customs Code
- DHA04400258900
Company information
- Manufacturer
- PILLING SURGICAL
- Manufacturer Country
- United States
- Authorized Representative
- SUNSHINE INSTRUMENT LTD.
Product details
- Intended Use
- A surgical instrument with a special function for cardiovascular surgery.
- 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
- Feb 07, 2006
- Expiry Date
- Feb 07, 2011
- Cancellation Date
- Nov 30, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Thunderbolt" aortic punch (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 05dec9f51beb42524754bc042db823e0 and manufactured by PILLING SURGICAL. The authorized representative in Taiwan is SUNSHINE INSTRUMENT LTD..
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