Taiwan FDA registration 0c64894cb7cb06e143a2b5a98170d440
“Promedon” Splentis POP Tissue Anchoring System
TW: “博美敦”絲布藍脫垂修補系統
Taiwan·Risk Class 3·MD·Promedon S.A.·Registered Nov 19, 2014 – Nov 19, 2024ExpiredRegistration details
- Analysis ID
- 0c64894cb7cb06e143a2b5a98170d440
- License Form
- Ministry of Health Medical Device Import No. 026790
- Customs Code
- DHA05602679001
Company information
- Manufacturer
- Promedon S.A.
- Manufacturer Country
- Argentina
- Authorized Representative
- Foresee Medical Ltd.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- l Devices for obstetrics and gynecology
- Product Type (Level 2)
- L5980 Surgical mesh for transvaginal pelvic organ prolapse treatment
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 19, 2014
- Expiry Date
- Nov 19, 2024
About this record
Access comprehensive regulatory information for “Promedon” Splentis POP Tissue Anchoring System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 0c64894cb7cb06e143a2b5a98170d440 and manufactured by Promedon S.A.. The authorized representative in Taiwan is Foresee Medical Ltd..
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