Taiwan FDA registration 78be7b45b90bbd23cee6e87ddf8ce016
"August Reuchlen" Manual Surgical instruments for general use (Non-Sterile)
TW: "阿格斯"一般手術用手動式器械(未滅菌)
Taiwan·Risk Class 1·MD·AUGUST REUCHLEN GMBH·Registered Dec 17, 2015 – Dec 17, 2020CancelledRegistration details
- Analysis ID
- 78be7b45b90bbd23cee6e87ddf8ce016
- License Form
- Ministry of Health Medical Device Import No. 015991
- Customs Code
- DHA09401599104
Company information
- Manufacturer
- AUGUST REUCHLEN GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- WELLONG INSTRUMENTS CO., LTD.
Product details
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I4800 General Surgery Manual Instrument
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 17, 2015
- Expiry Date
- Dec 17, 2020
- Cancellation Date
- Jun 16, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期未申請展延
About this record
Access comprehensive regulatory information for "August Reuchlen" Manual Surgical instruments for general use (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 78be7b45b90bbd23cee6e87ddf8ce016 and manufactured by AUGUST REUCHLEN GMBH. The authorized representative in Taiwan is WELLONG INSTRUMENTS CO., LTD..
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