Taiwan FDA registration 0427acddddccf81b9b091e6e4bebd1e4
“Aesculap” Elan 4 Power Instruments and Accessories
TW: “雅氏”怡然動力工具及其附件
Taiwan·Risk Class 2·MD·AESCULAP AG·Registered Jul 24, 2021 – Jul 24, 2026ExpiredRegistration details
- Analysis ID
- 0427acddddccf81b9b091e6e4bebd1e4
- License Form
- Ministry of Health Medical Device Import No. 034725
- Customs Code
- DHA05603472509
Company information
- Manufacturer
- AESCULAP AG
- Manufacturer Country
- Germany
- Authorized Representative
- B. BRAUN TAIWAN CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- 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
- Jul 24, 2021
- Expiry Date
- Jul 24, 2026
About this record
Access comprehensive regulatory information for “Aesculap” Elan 4 Power Instruments and Accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0427acddddccf81b9b091e6e4bebd1e4 and manufactured by AESCULAP AG. The authorized representative in Taiwan is B. BRAUN TAIWAN CO., LTD..
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