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Ingro’s Cannulate Screw - Taiwan Registration e448e82dde93bc699a449621f41f5dbe

Access comprehensive regulatory information for Ingro’s Cannulate Screw in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number e448e82dde93bc699a449621f41f5dbe and manufactured by INGROWTH BIOTECH CO., LTD.. The authorized representative in Taiwan is INGROWTH BIOTECH 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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e448e82dde93bc699a449621f41f5dbe
Registration Details
Taiwan FDA Registration: e448e82dde93bc699a449621f41f5dbe
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Device Details

Ingro’s Cannulate Screw
TW: 可成中空骨釘
Risk Class 3
MD
Cancelled

Registration Details

e448e82dde93bc699a449621f41f5dbe

Ministry of Health Medical Device Manufacturing No. 006681

Company Information

Taiwan, Province of China

Product Details

N Orthopedic devices

N3040 Smooth or threaded metal bone fixation

Produced in Taiwan, China

Dates and Status

Mar 26, 2020

Mar 26, 2025

May 14, 2021

Cancellation Information

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