Taiwan FDA registration 1b31842a9c063e0223365f5af6a7e378

"Di Cheng" introduction/drainage catheter and its accessories (unsterilized)

TW: “狄成”導入/引流導管及其附件 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·DI CHENG RUBBER INDUSTRIES INC.·Registered Dec 04, 2008 – Dec 04, 2013Cancelled
Registration details
Analysis ID
1b31842a9c063e0223365f5af6a7e378
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
DI CHENG RUBBER INDUSTRIES INC.
Product details
Intended Use
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.
Product Type (Level 1)
I General, Plastic Surgery and Dermatology
Product Type (Level 2)
I.4200 Incoming/Drainage Tubes and Accessories
Import Information
Domestic
Dates and status
Registration Date
Dec 04, 2008
Expiry Date
Dec 04, 2013
Cancellation Date
Dec 30, 2013
Cancellation information
Status
Logged out
Reason
自請註銷
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About this record

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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