Taiwan FDA registration 02291c65c883587dfa5044b419f30108
“NeoMedic” MINIMALLY INVASIVE PROLAPSE SYSTEM
TW: “尼奧麥迪克”蜜普思微創骨盆懸吊系統
Taiwan·Risk Class 3·MD·Desarrollo e Investigación Médica Aragonesa S.L.·Registered Apr 25, 2018 – Apr 25, 2028ActiveRegistration details
- Analysis ID
- 02291c65c883587dfa5044b419f30108
- License Form
- Ministry of Health Medical Device Import No. 030820
- Customs Code
- DHA05603082009
Company information
- Manufacturer
- Desarrollo e Investigación Médica Aragonesa S.L.
- Manufacturer Country
- Spain
- Authorized Representative
- Soar Medical Corp.
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
- Apr 25, 2018
- Expiry Date
- Apr 25, 2028
About this record
Access comprehensive regulatory information for “NeoMedic” MINIMALLY INVASIVE PROLAPSE SYSTEM in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 02291c65c883587dfa5044b419f30108 and manufactured by Desarrollo e Investigación Médica Aragonesa S.L.. The authorized representative in Taiwan is Soar Medical Corp..
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