Taiwan FDA registration 67d6bec5b55ac36b507684dbc910a2b0
Fibli Kaixun Rehabilitation Equipment and Accessories (Unsterilized)
TW: "菲布利凱訊"復健用裝具及配件(未滅菌)
Taiwan·Risk Class 1·FABRICATION ENTERPRISES INCORPORATED·Registered Jan 10, 2013 – Jan 10, 2028ActiveRegistration details
- Analysis ID
- 67d6bec5b55ac36b507684dbc910a2b0
- Customs Code
- DHA04401257801
Company information
- Manufacturer
- FABRICATION ENTERPRISES INCORPORATED
- Manufacturer Country
- United States
- Authorized Representative
- GOOD LINE INCORPORATION
Product details
- Intended Use
- Limited to the first level recognition range of medical equipment classification and grading management measures for prosthetics and accessories for accessories (O.3025).
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O.3025 義肢及裝具用附件
- Import Information
- import
Dates and status
- Registration Date
- Jan 10, 2013
- Expiry Date
- Jan 10, 2028
About this record
Access comprehensive regulatory information for Fibli Kaixun Rehabilitation Equipment and Accessories (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 67d6bec5b55ac36b507684dbc910a2b0 and manufactured by FABRICATION ENTERPRISES INCORPORATED. The authorized representative in Taiwan is GOOD LINE INCORPORATION.
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