Taiwan FDA registration a79840227819b680523fae212247ad92

"Kaberfi" Fikson intramedullary nail system

TW: “卡伯菲”菲克迅髓內釘系統
Taiwan flagTaiwan·Risk Class 2·CarboFix Orthopedics Ltd.·Registered Apr 29, 2013 – Apr 29, 2018Cancelled
Registration details
Analysis ID
a79840227819b680523fae212247ad92
Customs Code
DHA00602493600
Company information
Manufacturer Country
Israel
Authorized Representative
JOINSMART BIOMEDICAL COMPANY LIMITED
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
N Orthopedics
Product Type (Level 2)
N.3020 骨髓內固定桿
Import Information
import
Dates and status
Registration Date
Apr 29, 2013
Expiry Date
Apr 29, 2018
Cancellation Date
Dec 20, 2019
Cancellation information
Status
Logged out
Reason
未展延而逾期者
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About this record

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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