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"Sanyo" Enfi drainage catheter (unsterilized) - Taiwan Registration 54f5346f96cdf5463cbcac94b9a56ce2

Access comprehensive regulatory information for "Sanyo" Enfi drainage 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 54f5346f96cdf5463cbcac94b9a56ce2 and manufactured by SANYO POLYMER INDUSTRY CO., LTD.. The authorized representative in Taiwan is Huangfa Co., Ltd.

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.

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54f5346f96cdf5463cbcac94b9a56ce2
Registration Details
Taiwan FDA Registration: 54f5346f96cdf5463cbcac94b9a56ce2
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Device Details

"Sanyo" Enfi drainage catheter (unsterilized)
TW: "ไธ‰ๆด‹" ๆฉ่ฒๅผ•ๆตๅฐŽ็ฎก(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

54f5346f96cdf5463cbcac94b9a56ce2

DHA04400427401

Company Information

Product Details

I General, Plastic Surgery and Dermatology

I.4200 Incoming/Drainage Tubes and Accessories

import

Dates and Status

Apr 28, 2006

Apr 28, 2011

Oct 25, 2012

Cancellation Information

Logged out

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