Taiwan FDA registration fb3ac20a73042731190f0d837ee90bb5
"Ya'Arth" medical light source machine
TW: "雅氏" 醫用光源機
Taiwan·Risk Class 2·AESCULAP AG·Registered Nov 18, 2005 – Nov 18, 2020CancelledRegistration details
- Analysis ID
- fb3ac20a73042731190f0d837ee90bb5
- Customs Code
- DHA00601359308
Company information
- Manufacturer
- AESCULAP AG
- Manufacturer Country
- Germany
- Authorized Representative
- Taiwan Birlanc Co., Ltd
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.1500 Internal Scope and its accessories
- Import Information
- import
Dates and status
- Registration Date
- Nov 18, 2005
- Expiry Date
- Nov 18, 2020
- Cancellation Date
- Jul 15, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Ya'Arth" medical light source machine in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fb3ac20a73042731190f0d837ee90bb5 and manufactured by AESCULAP AG. The authorized representative in Taiwan is Taiwan Birlanc Co., Ltd.
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