Taiwan FDA registration 30a8be4216bf38c6cac17f9e7ba1d786
"Peimixin" manual instruments for general surgery (unsterilized)
TW: “培蜜星”一般手術用手動式器械 (未滅菌)
Taiwan·Risk Class 1·PRIMESTAR INSTRUMENTS·Registered Apr 27, 2011 – Apr 27, 2016CancelledRegistration details
- Analysis ID
- 30a8be4216bf38c6cac17f9e7ba1d786
- Customs Code
- DHA04401026700
Company information
- Manufacturer
- PRIMESTAR INSTRUMENTS
- Manufacturer Country
- Pakistan
- Authorized Representative
- Apricot Strong, Inc
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, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4800 Hand Instruments for General Surgery
- Import Information
- import
Dates and status
- Registration Date
- Apr 27, 2011
- Expiry Date
- Apr 27, 2016
- Cancellation Date
- Aug 13, 2018
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Peimixin" manual instruments for general 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 30a8be4216bf38c6cac17f9e7ba1d786 and manufactured by PRIMESTAR INSTRUMENTS. The authorized representative in Taiwan is Apricot Strong, 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