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"Kaberfi" Fikson intramedullary nail system - Taiwan Registration 29e0d63e17be2c4a7a29ed9961767ee7

Access comprehensive regulatory information for "Kaberfi" Fikson intramedullary nail system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 29e0d63e17be2c4a7a29ed9961767ee7 and manufactured by CarboFix Orthopedics Ltd.. The authorized representative in Taiwan is JOINSMART BIOMEDICAL COMPANY LIMITED.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including CarboFix Orthopedics Ltd., and 1 recent registrations in the same category. 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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29e0d63e17be2c4a7a29ed9961767ee7
Registration Details
Taiwan FDA Registration: 29e0d63e17be2c4a7a29ed9961767ee7
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Device Details

"Kaberfi" Fikson intramedullary nail system
TW: โ€œๅกไผฏ่ฒโ€่ฒๅ…‹่ฟ…้ซ“ๅ…ง้‡˜็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

29e0d63e17be2c4a7a29ed9961767ee7

DHA00602516605

Company Information

Israel

Product Details

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

N Orthopedics

N.3020 ้ชจ้ซ“ๅ…งๅ›บๅฎšๆกฟ

import

Dates and Status

Jul 06, 2013

Jul 06, 2018

Jun 07, 2022

Cancellation Information

Logged out

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