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"Di Cheng" introduction/drainage catheter and its accessories (unsterilized) - Taiwan Registration 600071d07b71494cb8425aef95fde2ed

Access comprehensive regulatory information for "Di Cheng" introduction/drainage catheter and its accessories (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 600071d07b71494cb8425aef95fde2ed 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, 1 companies making similar products including DI CHENG RUBBER INDUSTRIES INC., and 1 recent registrations in the same category. 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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600071d07b71494cb8425aef95fde2ed
Registration Details
Taiwan FDA Registration: 600071d07b71494cb8425aef95fde2ed
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Device Details

"Di Cheng" introduction/drainage catheter and its accessories (unsterilized)
TW: "็‹„ๆˆ" ๅฐŽๅ…ฅ/ๅผ•ๆตๅฐŽ็ฎกๅŠๅ…ถ้™„ไปถ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

600071d07b71494cb8425aef95fde2ed

Company Information

Taiwan, Province of China

Product Details

Limited to the first level of identification scope of the Measures for the Classification and Grading of Medical Devices "Introduction/Drainage Catheters and Their Accessories (I.4200)".

I General, Plastic Surgery and Dermatology

I.4200 Incoming/Drainage Tubes and Accessories

Domestic

Dates and Status

Dec 18, 2013

Dec 18, 2023

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