Pure Global

Cenefom foam for nasal hemostasis (sterilized) - Taiwan Registration b0c0b6df5d70619d9603ed3d13ac8c68

Access comprehensive regulatory information for Cenefom foam for nasal hemostasis (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b0c0b6df5d70619d9603ed3d13ac8c68 and manufactured by CENEFOM CORP.. The authorized representative in Taiwan is CENEFOM 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 Database
Powered by Pure Global AI
89,000+ Devices
b0c0b6df5d70619d9603ed3d13ac8c68
Registration Details
Taiwan FDA Registration: b0c0b6df5d70619d9603ed3d13ac8c68
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

Cenefom foam for nasal hemostasis (sterilized)
TW: Cenefom ้ผปๆญข่ก€็”จๆณกๆฃ‰ (ๆป…่Œ)
Risk Class 1

Registration Details

b0c0b6df5d70619d9603ed3d13ac8c68

Company Information

Taiwan, Province of China

Product Details

Limited to the first level of classification and grading management of medical devices "external use of non-absorbent gauze or sponge balls (I.4014)" identification range.

I General, Plastic Surgery and Dermatology

I.4014 Non-absorbent cloth or sea balls are used externally

ๅœ‹็”ข;; QMS/QSD

Dates and Status

Jan 24, 2017

Jan 24, 2027