Taiwan FDA registration 5f3e1e100bfc3fee4bfa60c0bd4e2fd9
“Omnia” PTFE Suture
TW: “歐尼雅”非吸收聚四氟乙烯縫合線
Taiwan·Risk Class 2·MD·OMNIA·Registered May 20, 2022 – May 20, 2027ActiveRegistration details
- Analysis ID
- 5f3e1e100bfc3fee4bfa60c0bd4e2fd9
- License Form
- Ministry of Health Medical Device Import No. 035480
- Customs Code
- DHA05603548000
Company information
- Manufacturer
- OMNIA
- Manufacturer Country
- Italy
- Authorized Representative
- YUYING BIOTECHNOLOGY CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I5035 Non-absorbent expanded PTFE surgical suture
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 20, 2022
- Expiry Date
- May 20, 2027
About this record
Access comprehensive regulatory information for “Omnia” PTFE Suture in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5f3e1e100bfc3fee4bfa60c0bd4e2fd9 and manufactured by OMNIA. The authorized representative in Taiwan is YUYING BIOTECHNOLOGY CO., LTD..
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