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"Greer" Wound Drainage Devices (Non-terile) - Taiwan Registration 814fbb125ab7d408e5f2a190a9fb42ab

Access comprehensive regulatory information for "Greer" Wound Drainage Devices (Non-terile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 814fbb125ab7d408e5f2a190a9fb42ab and manufactured by Greer Medical Inc. The authorized representative in Taiwan is LANCET MEDICAL ENTERPRISE 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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814fbb125ab7d408e5f2a190a9fb42ab
Registration Details
Taiwan FDA Registration: 814fbb125ab7d408e5f2a190a9fb42ab
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Device Details

"Greer" Wound Drainage Devices (Non-terile)
TW: "ๆ ผ็‘ž"ๅ‚ทๅฃๅผ•ๆต่ฃ็ฝฎ(ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

814fbb125ab7d408e5f2a190a9fb42ab

Ministry of Health Medical Device Import No. 103604

DHA09410360401

Company Information

United States

Product Details

I General and plastic surgical devices

I4200 Introduction/drainage catheters and their accessories

Imported from abroad

Dates and Status

Jul 30, 2014

Jul 30, 2019

Jul 15, 2022

Cancellation Information

Logged out

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