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“Cytoplast” PTFE Suture - Taiwan Registration 03e52e70f3bfa7efef60fe23e6b43f05

Access comprehensive regulatory information for “Cytoplast” 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 03e52e70f3bfa7efef60fe23e6b43f05 and manufactured by OSTEOGENICS BIOMEDICAL, INC.. The authorized representative in Taiwan is OSSTEM CORPORATION.

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.

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03e52e70f3bfa7efef60fe23e6b43f05
Registration Details
Taiwan FDA Registration: 03e52e70f3bfa7efef60fe23e6b43f05
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Device Details

“Cytoplast” PTFE Suture
TW: “山多普斯”非吸收聚四氟乙烯縫合線
Risk Class 2
MD

Registration Details

03e52e70f3bfa7efef60fe23e6b43f05

Ministry of Health Medical Device Import No. 030668

DHA05603066803

Company Information

United States

Product Details

For details, it is Chinese approved copy of the imitation order

I General and plastic surgical devices

I5035 Non-absorbent expanded PTFE surgical sutures

Imported from abroad

Dates and Status

Dec 29, 2017

Dec 29, 2027