Taiwan FDA registration df690350515738a4b70af93d788538e0
“Aesculap” Urethral dilator accessories (Non-sterile)
TW: “雅氏” 尿道擴張器附件(未滅菌)
Taiwan·Risk Class 1·MD·AESCULAP AG·Registered Jul 17, 2020 – Jul 17, 2025ExpiredRegistration details
- Analysis ID
- df690350515738a4b70af93d788538e0
- License Form
- Ministry of Health Medical Device Import No. 021753
- Customs Code
- DHA09402175300
Company information
- Manufacturer
- AESCULAP AG
- Manufacturer Country
- Germany
- Authorized Representative
- B. BRAUN TAIWAN CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of "urethral dilator (H.5520)" of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- H Gastroenterology-urology devices
- Product Type (Level 2)
- H5520 Urethral dilators
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 17, 2020
- Expiry Date
- Jul 17, 2025
About this record
Access comprehensive regulatory information for “Aesculap” Urethral dilator accessories (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 df690350515738a4b70af93d788538e0 and manufactured by AESCULAP AG. The authorized representative in Taiwan is B. BRAUN TAIWAN CO., LTD..
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