Taiwan FDA registration 38d9a701995715364487a56229fb33d1
“NeoMedic” SURELIFT CONTASURE PROLAPSE SYSTEM
TW: “尼奧麥迪克”舒兒莉芙特骨盆懸吊系統
Registration details
- Analysis ID
- 38d9a701995715364487a56229fb33d1
- License Form
- Ministry of Health Medical Device Import No. 028560
- Customs Code
- DHA05602856004
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
- May 03, 2016
- Expiry Date
- May 03, 2026
About this record
Access comprehensive regulatory information for “NeoMedic” SURELIFT CONTASURE 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 38d9a701995715364487a56229fb33d1 and manufactured by Desarrollo e Investigación Médica Aragonesa S.L.. The authorized representative in Taiwan is Soar Medical Corp..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices