Pure Global

“Omnia” PTFE Suture - Taiwan Registration 5f3e1e100bfc3fee4bfa60c0bd4e2fd9

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..

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 Database
Powered by Pure Global AI
89,000+ Devices
5f3e1e100bfc3fee4bfa60c0bd4e2fd9
Registration Details
Taiwan FDA Registration: 5f3e1e100bfc3fee4bfa60c0bd4e2fd9
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“Omnia” PTFE Suture
TW: “歐尼雅”非吸收聚四氟乙烯縫合線
Risk Class 2
MD

Registration Details

5f3e1e100bfc3fee4bfa60c0bd4e2fd9

Ministry of Health Medical Device Import No. 035480

DHA05603548000

Company Information

Italy

Product Details

Details are as detailed as approved Chinese instructions

I General, Plastic Surgery and Dermatology

I5035 Non-absorbent expanded PTFE surgical suture

Imported from abroad

Dates and Status

May 20, 2022

May 20, 2027