Taiwan FDA registration fdb90eaee2a49fa2d1562786e2671d9e
“Aesculap” Elan 4Pneumatic System
TW: “雅氏”怡然氣動工具系統
Taiwan·Risk Class 2·MD·AESCULAP AG·Registered Jun 22, 2019 – Jun 22, 2024ExpiredRegistration details
- Analysis ID
- fdb90eaee2a49fa2d1562786e2671d9e
- License Form
- Ministry of Health Medical Device Import No. 032695
- Customs Code
- DHA05603269503
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)
- K4370 Pneumatic Head Cranial Drill Motor
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 22, 2019
- Expiry Date
- Jun 22, 2024
About this record
Access comprehensive regulatory information for “Aesculap” Elan 4Pneumatic System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fdb90eaee2a49fa2d1562786e2671d9e and manufactured by AESCULAP AG. The authorized representative in Taiwan is B. BRAUN TAIWAN CO., LTD..
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