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“Stryker” Smartlock Hybrid MMF System - Taiwan Registration 97531ddf0bfbb004c0cea619d3917762

Access comprehensive regulatory information for “Stryker” Smartlock Hybrid MMF System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 97531ddf0bfbb004c0cea619d3917762 and manufactured by STRYKER LEIBINGER GMBH & CO.KG. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).

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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97531ddf0bfbb004c0cea619d3917762
Registration Details
Taiwan FDA Registration: 97531ddf0bfbb004c0cea619d3917762
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Device Details

“Stryker” Smartlock Hybrid MMF System
TW: “史賽克”高明顎骨鎖定系統
Risk Class 2
MD

Registration Details

97531ddf0bfbb004c0cea619d3917762

Ministry of Health Medical Device Import No. 032853

DHA05603285308

Company Information

Product Details

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

F Dental devices

F4760 bone plate

Imported from abroad

Dates and Status

Sep 27, 2019

Sep 27, 2024