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“PEGA” Gap Endo Exo Medullary System - Taiwan Registration 0206abb4e01b03ef01e54eb9a7f0d405

Access comprehensive regulatory information for “PEGA” Gap Endo Exo Medullary System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0206abb4e01b03ef01e54eb9a7f0d405 and manufactured by PEGA MEDICAL INC.. The authorized representative in Taiwan is EULOGIUMS 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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0206abb4e01b03ef01e54eb9a7f0d405
Registration Details
Taiwan FDA Registration: 0206abb4e01b03ef01e54eb9a7f0d405
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Device Details

“PEGA” Gap Endo Exo Medullary System
TW: “沛佳”內外髓內釘系統
Risk Class 2
MD

Registration Details

0206abb4e01b03ef01e54eb9a7f0d405

Ministry of Health Medical Device Import No. 031173

DHA05603117307

Company Information

Canada

Product Details

For details, it is Chinese approved copy of the imitation order

N Orthopedic devices

N3020 Intra-bone marrow fixation rod

Imported from abroad

Dates and Status

Jun 08, 2018

Jun 08, 2028