Taiwan FDA registration 5e0932d11b20f883a854ebfcc6b673fd
“Lance” Surgical Blades (Non-Sterile)
TW: “藍斯” 手術刀片 (未滅菌)
Taiwan·Risk Class 1·MD·SWANN-MORTON LTD.·Registered Mar 27, 2019 – Mar 27, 2024ExpiredRegistration details
- Analysis ID
- 5e0932d11b20f883a854ebfcc6b673fd
- License Form
- Ministry of Health Medical Device Import No. 020243
- Customs Code
- DHA09402024301
Company information
- Manufacturer
- SWANN-MORTON LTD.
- Manufacturer Country
- United Kingdom
- Authorized Representative
- PANPAC MEDICAL CORPORATION
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 and plastic surgical devices
- Product Type (Level 2)
- I4800 General Surgery Manual Instrument
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 27, 2019
- Expiry Date
- Mar 27, 2024
About this record
Access comprehensive regulatory information for “Lance” Surgical Blades (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 5e0932d11b20f883a854ebfcc6b673fd and manufactured by SWANN-MORTON LTD.. The authorized representative in Taiwan is PANPAC MEDICAL CORPORATION.
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