Taiwan FDA registration fc2ea6274035cb865614f6fcfcb2e842
"Feno" long back plate (unsterilized)
TW: "費諾"長背板(未滅菌)
Taiwan·Risk Class 1·FERNO-WASHINGTON, INC.·Registered Sep 13, 2011 – Sep 13, 2026CancelledRegistration details
- Analysis ID
- fc2ea6274035cb865614f6fcfcb2e842
- Customs Code
- DHA04401006807
Company information
- Manufacturer
- FERNO-WASHINGTON, INC.
- Manufacturer Country
- United States
- Authorized Representative
- ADEPT GENERAL CORP.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Torso Equipment (O.3490)".
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.6900 Hand-held stretcher
- Import Information
- import
Dates and status
- Registration Date
- Sep 13, 2011
- Expiry Date
- Sep 13, 2026
- Cancellation Date
- Sep 30, 2021
Cancellation information
- Status
- Logged out
- Reason
- 轉為登錄字號
About this record
Access comprehensive regulatory information for "Feno" long back plate (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number fc2ea6274035cb865614f6fcfcb2e842 and manufactured by FERNO-WASHINGTON, INC.. The authorized representative in Taiwan is ADEPT GENERAL CORP..
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