Pure Global

"Di Cheng" nasal oxygen catheter (unsterilized) - Taiwan Registration 88f2cab4cf0d28fbd3818365e29f190f

Access comprehensive regulatory information for "Di Cheng" nasal oxygen catheter (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 88f2cab4cf0d28fbd3818365e29f190f and manufactured by DI CHENG RUBBER INDUSTRIES INC.. The authorized representative in Taiwan is DI CHENG RUBBER INDUSTRIES INC..

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
88f2cab4cf0d28fbd3818365e29f190f
Registration Details
Taiwan FDA Registration: 88f2cab4cf0d28fbd3818365e29f190f
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Di Cheng" nasal oxygen catheter (unsterilized)
TW: "็‹„ๆˆ" ็ถ“้ผปๆฐงๆฐฃๅฐŽ็ฎก (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

88f2cab4cf0d28fbd3818365e29f190f

Company Information

Taiwan, Province of China

Product Details

It is limited to the first level of identification scope of the "Nasal Oxygen Catheter (D.5350)" of the Administrative Measures for the Classification and Grading of Medical Devices.

D Anesthesiology

D.5350 Nasal oxygen catheters

Domestic

Dates and Status

Dec 18, 2013

Dec 18, 2023