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"Kaberfi" Fikson intramedullary nail system - Taiwan Registration a79840227819b680523fae212247ad92

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 a79840227819b680523fae212247ad92 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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a79840227819b680523fae212247ad92
Registration Details
Taiwan FDA Registration: a79840227819b680523fae212247ad92
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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

a79840227819b680523fae212247ad92

DHA00602493600

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

Apr 29, 2013

Apr 29, 2018

Dec 20, 2019

Cancellation Information

Logged out

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