Taiwan FDA registration 814fbb125ab7d408e5f2a190a9fb42ab
"Greer" Wound Drainage Devices (Non-terile)
TW: "格瑞"傷口引流裝置(未滅菌)
Taiwan·Risk Class 1·MD·Greer Medical Inc·Registered Jul 30, 2014 – Jul 30, 2019CancelledRegistration details
- Analysis ID
- 814fbb125ab7d408e5f2a190a9fb42ab
- License Form
- Ministry of Health Medical Device Import No. 103604
- Customs Code
- DHA09410360401
Company information
- Manufacturer
- Greer Medical Inc
- Manufacturer Country
- United States
- Authorized Representative
- LANCET MEDICAL ENTERPRISE CO., LTD.
Product details
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I4200 Introduction/drainage catheters and their accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 30, 2014
- Expiry Date
- Jul 30, 2019
- 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 "Greer" Wound Drainage Devices (Non-terile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 814fbb125ab7d408e5f2a190a9fb42ab and manufactured by Greer Medical Inc. The authorized representative in Taiwan is LANCET MEDICAL ENTERPRISE CO., LTD..
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