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“Gyrus”Prosthesis modification instrument for ossicular replacement surgery(Non-sterile) - Taiwan Registration 7a075493a0522037301b02e7167fc397

Access comprehensive regulatory information for “Gyrus”Prosthesis modification instrument for ossicular replacement surgery(Non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 7a075493a0522037301b02e7167fc397 and manufactured by GYRUS MEDICAL GMBH. The authorized representative in Taiwan is Yuanyou Industrial 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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7a075493a0522037301b02e7167fc397
Registration Details
Taiwan FDA Registration: 7a075493a0522037301b02e7167fc397
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Device Details

“Gyrus”Prosthesis modification instrument for ossicular replacement surgery(Non-sterile)
TW: “吉洛氏”聽小骨置換物修正用器械 (未滅菌)
Risk Class 1
MD
Cancelled

Registration Details

7a075493a0522037301b02e7167fc397

Ministry of Health Medical Device Import No. 013969

DHA09401396901

Company Information

Germany

Product Details

G ENT device

G3540 Instrument for Hearing Bone Replacement Correction

Imported from abroad

Dates and Status

Mar 18, 2014

Mar 18, 2019

Aug 05, 2022

Cancellation Information

Logged out

未展延而逾期者