Taiwan FDA registration 59574022f382f385c8330c1ad0b6dbaa
"Pomedon" abruptly plastic artificial
TW: “博美敦”突勃可塑性人工陰莖
Taiwan·Risk Class 2·Promedon S.A.·Registered Oct 31, 2014 – Oct 31, 2029ActiveRegistration details
- Analysis ID
- 59574022f382f385c8330c1ad0b6dbaa
- Customs Code
- DHA05602676703
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)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.3630 硬式陰莖植入物
- Import Information
- import
Dates and status
- Registration Date
- Oct 31, 2014
- Expiry Date
- Oct 31, 2029
About this record
Access comprehensive regulatory information for "Pomedon" abruptly plastic artificial in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 59574022f382f385c8330c1ad0b6dbaa and manufactured by Promedon S.A.. The authorized representative in Taiwan is Foresee Medical Ltd..
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