Taiwan FDA registration 0206abb4e01b03ef01e54eb9a7f0d405
“PEGA” Gap Endo Exo Medullary System
TW: “沛佳”內外髓內釘系統
Taiwan·Risk Class 2·MD·PEGA MEDICAL INC.·Registered Jun 08, 2018 – Jun 08, 2028ActiveRegistration details
- Analysis ID
- 0206abb4e01b03ef01e54eb9a7f0d405
- License Form
- Ministry of Health Medical Device Import No. 031173
- Customs Code
- DHA05603117307
Company information
- Manufacturer
- PEGA MEDICAL INC.
- Manufacturer Country
- Canada
- Authorized Representative
- EULOGIUMS CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- N Orthopedic devices
- Product Type (Level 2)
- N3020 Intra-bone marrow fixation rod
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 08, 2018
- Expiry Date
- Jun 08, 2028
About this record
Access comprehensive regulatory information for “PEGA” Gap Endo Exo Medullary System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0206abb4e01b03ef01e54eb9a7f0d405 and manufactured by PEGA MEDICAL INC.. The authorized representative in Taiwan is EULOGIUMS CO., LTD..
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