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"Spite" Romeo Pader interspinal system - Taiwan Registration ac5d217398e6e8fb32f29f080c85df2c

Access comprehensive regulatory information for "Spite" Romeo Pader interspinal system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ac5d217398e6e8fb32f29f080c85df2c and manufactured by SPINEART SA;; ALPES CN SAS. 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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ac5d217398e6e8fb32f29f080c85df2c
Registration Details
Taiwan FDA Registration: ac5d217398e6e8fb32f29f080c85df2c
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Device Details

"Spite" Romeo Pader interspinal system
TW: โ€œๅธไฝฐ็‰นโ€็พ…ๅฏ†ๆญๅธ•ๅพท่„Š็ช้–“็ณป็ตฑ
Risk Class 2

Registration Details

ac5d217398e6e8fb32f29f080c85df2c

DHA00602474200

Company Information

France;;Switzerland

Product Details

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

N Orthopedics

N.3060 ๆคŽ้ซ”้–“ไน‹่„ŠๆคŽ็Ÿฏๆญฃๅ›บๅฎš็‰ฉ

import

Dates and Status

Feb 20, 2013

Feb 20, 2028