Taiwan FDA registration 23179d8dafe7f82085a519506f052d1f
“OMNIPORE” Surgical Implants
TW: "傲密補" 植入式人工骨
Registration details
- Analysis ID
- 23179d8dafe7f82085a519506f052d1f
- License Form
- Ministry of Health Medical Device Import No. 028374
- Customs Code
- DHA05602837407
Company information
- Manufacturer
- MATRIX SURGICAL HOLDINGS, LLC
- Manufacturer Country
- United States
- Authorized Representative
- Beleli Biotechnology Co., Ltd
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I3500 Implant material for PTFE containing carbon fiber synthetics
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 14, 2016
- Expiry Date
- Apr 14, 2026
About this record
Access comprehensive regulatory information for “OMNIPORE” Surgical Implants in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 23179d8dafe7f82085a519506f052d1f and manufactured by MATRIX SURGICAL HOLDINGS, LLC. The authorized representative in Taiwan is Beleli Biotechnology Co., Ltd.
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