Taiwan FDA registration ea8f95aa91592392c3e516495dc629bf
“Aesculap” Elan 4 electro system
TW: “雅氏”怡然電動工具系統
Taiwan·Risk Class 2·MD·AESCULAP AG·Registered Dec 28, 2017 – Dec 28, 2027ActiveRegistration details
- Analysis ID
- ea8f95aa91592392c3e516495dc629bf
- License Form
- Ministry of Health Medical Device Import No. 030663
- Customs Code
- DHA05603066306
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)
- K Devices for neuroscience
- Product Type (Level 2)
- K4310 Power Simple Head Cap, File, Ring Saw and Its Accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 28, 2017
- Expiry Date
- Dec 28, 2027
About this record
Access comprehensive regulatory information for “Aesculap” Elan 4 electro system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ea8f95aa91592392c3e516495dc629bf and manufactured by AESCULAP AG. The authorized representative in Taiwan is B. BRAUN TAIWAN CO., LTD..
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