Taiwan FDA registration 2a7cf9c5952a6e4c0a5e5658cf5fc108

"Smith" Jaco intravenous indwelling needle

TW: “史密斯”杰可靜脈留置針
Taiwan flagTaiwan·Risk Class 2·SMITHS MEDICAL ITALIA S.R.L·Registered Nov 16, 2010 – Nov 16, 2020Cancelled
Registration details
Analysis ID
2a7cf9c5952a6e4c0a5e5658cf5fc108
Customs Code
DHA00602170301
Company information
Manufacturer Country
Italy
Authorized Representative
RADIANT MEDICAL COMPANY
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
J General hospital and personal use equipment
Product Type (Level 2)
J.5200 Endovascular catheters
Import Information
import
Dates and status
Registration Date
Nov 16, 2010
Expiry Date
Nov 16, 2020
Cancellation Date
Aug 05, 2022
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 "Smith" Jaco intravenous indwelling needle in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2a7cf9c5952a6e4c0a5e5658cf5fc108 and manufactured by SMITHS MEDICAL ITALIA S.R.L. The authorized representative in Taiwan is RADIANT MEDICAL COMPANY.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including SMITHS MEDICAL ITALIA S.R.L, 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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