Taiwan FDA registration 0dd645b7f2fef9b0e232829b6edc62ad
Kendalu In vitro assembly of lower limb prosthetics (unsterilized)
TW: 肯達路 體外組裝下肢義肢(未滅菌)
Taiwan·Risk Class 1·KEN DALL ENTERPRISE CO., LTD.·Registered Apr 07, 2023 – Apr 07, 2028ActiveRegistration details
- Analysis ID
- 0dd645b7f2fef9b0e232829b6edc62ad
Company information
- Manufacturer
- KEN DALL ENTERPRISE CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- KEN DALL ENTERPRISE CO., LTD.
Product details
- Intended Use
- Limited to the classification and grading management method of medical equipment, in vitro assembly of lower limb prosthetics (O.3500) first level recognition range.
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O.3500 shades
- Import Information
- 國產;; QMS/QSD
Dates and status
- Registration Date
- Apr 07, 2023
- Expiry Date
- Apr 07, 2028
About this record
Access comprehensive regulatory information for Kendalu In vitro assembly of lower limb prosthetics (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0dd645b7f2fef9b0e232829b6edc62ad and manufactured by KEN DALL ENTERPRISE CO., LTD.. The authorized representative in Taiwan is KEN DALL ENTERPRISE CO., LTD..
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