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“Synthes” VA-LCP Condylar Plate - Taiwan Registration 8af24486b120b27cbee22908aa15a0cc

Access comprehensive regulatory information for “Synthes” VA-LCP Condylar Plate in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8af24486b120b27cbee22908aa15a0cc and manufactured by SYNTHES GMBH. The authorized representative in Taiwan is JOHNSON & JOHNSON MEDICAL TAIWAN 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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8af24486b120b27cbee22908aa15a0cc
Registration Details
Taiwan FDA Registration: 8af24486b120b27cbee22908aa15a0cc
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Device Details

“Synthes” VA-LCP Condylar Plate
TW: “信迪思”多角度鎖定加壓股骨髁骨板
Risk Class 2
MD

Registration Details

8af24486b120b27cbee22908aa15a0cc

Ministry of Health Medical Device Import No. 030337

DHA05603033706

Company Information

Switzerland

Product Details

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

N Orthopedic devices

N3030 Single or multi-metal bone fixation device and accessories

Imported from abroad

Dates and Status

Oct 12, 2017

Oct 12, 2027