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“SPINEART” JULIET LL-T Lumbar Cage - Taiwan Registration 838f63742944d9a63fa9fc56f4d3e677

Access comprehensive regulatory information for “SPINEART” JULIET LL-T Lumbar Cage in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 838f63742944d9a63fa9fc56f4d3e677 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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838f63742944d9a63fa9fc56f4d3e677
Registration Details
Taiwan FDA Registration: 838f63742944d9a63fa9fc56f4d3e677
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Device Details

“SPINEART” JULIET LL-T Lumbar Cage
TW: “司佰特”茱麗葉腰椎融合器
Risk Class 2
MD

Registration Details

838f63742944d9a63fa9fc56f4d3e677

Ministry of Health Medical Device Import No. 028202

DHA05602820204

Company Information

Switzerland

Product Details

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

N Orthopedic devices

N3080 Interbody fusion device

Imported from abroad

Dates and Status

Feb 23, 2016

Feb 23, 2021