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“SPINEART” ROMEO 2 Lumbar Posterior Osteosynthesis System - Taiwan Registration 0577c8014b9f6f36099446efabaaac49

Access comprehensive regulatory information for “SPINEART” ROMEO 2 Lumbar Posterior Osteosynthesis System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0577c8014b9f6f36099446efabaaac49 and manufactured by SPINEART SA. The authorized representative in Taiwan is JOINSMART BIOMEDICAL COMPANY LIMITED.

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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0577c8014b9f6f36099446efabaaac49
Registration Details
Taiwan FDA Registration: 0577c8014b9f6f36099446efabaaac49
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Device Details

“SPINEART” ROMEO 2 Lumbar Posterior Osteosynthesis System
TW: “司佰特”羅密歐腰椎後路固定系統
Risk Class 2
MD

Registration Details

0577c8014b9f6f36099446efabaaac49

Ministry of Health Medical Device Import No. 033853

DHA05603385300

Company Information

Switzerland

Product Details

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

N Orthopedic devices

N3070 Pedicle screw system

Imported from abroad

Dates and Status

Sep 08, 2020

Sep 08, 2025