Taiwan FDA registration 29e0d63e17be2c4a7a29ed9961767ee7

"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 Jul 06, 2013 – Jul 06, 2018Cancelled
Registration details
Analysis ID
29e0d63e17be2c4a7a29ed9961767ee7
Customs Code
DHA00602516605
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
Jul 06, 2013
Expiry Date
Jul 06, 2018
Cancellation Date
Jun 07, 2022
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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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 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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