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"Di Cheng" introduction/drainage catheter and its accessories (unsterilized) - Taiwan Registration 1b31842a9c063e0223365f5af6a7e378

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 1b31842a9c063e0223365f5af6a7e378 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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1b31842a9c063e0223365f5af6a7e378
Registration Details
Taiwan FDA Registration: 1b31842a9c063e0223365f5af6a7e378
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Device Details

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

Registration Details

1b31842a9c063e0223365f5af6a7e378

Company Information

Taiwan, Province of China

Product Details

Limited to the scope of Grade 1 identification of "Introduction/Drainage Catheters and Their Accessories (I.4200)" under the Measures for the Administration of Medical Devices.

I General, Plastic Surgery and Dermatology

I.4200 Incoming/Drainage Tubes and Accessories

Domestic

Dates and Status

Dec 04, 2008

Dec 04, 2013

Dec 30, 2013

Cancellation Information

Logged out

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