Taiwan FDA registration 02f894a4e351e62b6a80700edc425662
“Premier”Manual surgical instrument for general use (Non-Sterile)
TW: “普密爾”一般手術用手動式器械 (未滅菌)
Taiwan·Risk Class 1·MD·PREMIER MEDICAL PRODUCTS·Registered Aug 26, 2013 – Aug 26, 2018CancelledRegistration details
- Analysis ID
- 02f894a4e351e62b6a80700edc425662
- License Form
- Ministry of Health Medical Device Import No. 013332
- Customs Code
- DHA09401333206
Company information
- Manufacturer
- PREMIER MEDICAL PRODUCTS
- Manufacturer Country
- United States
- Authorized Representative
- LYRA LTD.
Product details
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I4800 General Surgery Manual Instrument
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 26, 2013
- Expiry Date
- Aug 26, 2018
- Cancellation Date
- Jul 15, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for “Premier”Manual surgical instrument for general use (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 02f894a4e351e62b6a80700edc425662 and manufactured by PREMIER MEDICAL PRODUCTS. The authorized representative in Taiwan is LYRA 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