Taiwan FDA registration 9c78673a0e139524431df4db2af35989
"Aloft" is a pneumatic multi-haired suture clamp with titanium pneumatics
TW: “雅氏”巧掄鈦金屬氣動可重複使用多發式縫合夾
Taiwan·Risk Class 2·AESCULAP AG·Registered Mar 28, 2019 – Mar 28, 2029ActiveRegistration details
- Analysis ID
- 9c78673a0e139524431df4db2af35989
- Customs Code
- DHA05603235801
Company information
- Manufacturer
- AESCULAP AG
- Manufacturer Country
- Germany
- Authorized Representative
- B. BRAUN TAIWAN CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4300 Implantable Clips
- Import Information
- import
Dates and status
- Registration Date
- Mar 28, 2019
- Expiry Date
- Mar 28, 2029
About this record
Access comprehensive regulatory information for "Aloft" is a pneumatic multi-haired suture clamp with titanium pneumatics in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9c78673a0e139524431df4db2af35989 and manufactured by AESCULAP AG. The authorized representative in Taiwan is B. BRAUN TAIWAN 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