Taiwan FDA registration 4f5780299da9551b07ea5169c76aade4
”SEINEN” Instrument case (Non-sterile)
TW: ”喜能” 器械盒 (未滅菌)
Taiwan·Risk Class 1·MD·AYGUN CERRAHI ALETER.A.S·Registered Jun 08, 2020 – Jun 08, 2025ExpiredRegistration details
- Analysis ID
- 4f5780299da9551b07ea5169c76aade4
- License Form
- Ministry of Health Medical Device Import No. 021623
- Customs Code
- DHA09402162300
Company information
- Manufacturer
- AYGUN CERRAHI ALETER.A.S
- Manufacturer Country
- Turkey
- Authorized Representative
- Yuhong Medical Materials Co., Ltd
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
- Jun 08, 2020
- Expiry Date
- Jun 08, 2025
About this record
Access comprehensive regulatory information for ”SEINEN” Instrument case (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 4f5780299da9551b07ea5169c76aade4 and manufactured by AYGUN CERRAHI ALETER.A.S. The authorized representative in Taiwan is Yuhong Medical Materials Co., 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