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"Schnee-Fai" Introduction/drainage catheters and their accessories (sterilization) - Taiwan Registration 29ed7fd71cab0e7483289a138fd24728

Access comprehensive regulatory information for "Schnee-Fai" Introduction/drainage catheters and their accessories (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 29ed7fd71cab0e7483289a138fd24728 and manufactured by NYPRO PRECISION ASSEMBLIES DE MEXICO S.A. DE C.V.. The authorized representative in Taiwan is SMITH & NEPHEW ( OVERSEAS ) LIMITED, TAIWAN BRANCH (U.K.).

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29ed7fd71cab0e7483289a138fd24728
Registration Details
Taiwan FDA Registration: 29ed7fd71cab0e7483289a138fd24728
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Device Details

"Schnee-Fai" Introduction/drainage catheters and their accessories (sterilization)
TW: "ๅฒ่€่ผ" ๅฐŽๅ…ฅ/ๅผ•ๆตๅฐŽ็ฎกๅŠๅ…ถ้™„ไปถ(ๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

29ed7fd71cab0e7483289a138fd24728

DHA04401046402

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

QMS/QSD;; ่ผธๅ…ฅ

Dates and Status

Jun 10, 2011

Jun 10, 2016

Jun 25, 2018

Cancellation Information

Logged out

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