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"Smith" Jaco intravenous indwelling needle - Taiwan Registration 2a7cf9c5952a6e4c0a5e5658cf5fc108

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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2a7cf9c5952a6e4c0a5e5658cf5fc108
Registration Details
Taiwan FDA Registration: 2a7cf9c5952a6e4c0a5e5658cf5fc108
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Device Details

"Smith" Jaco intravenous indwelling needle
TW: โ€œๅฒๅฏ†ๆ–ฏโ€ๆฐๅฏ้œ่„ˆ็•™็ฝฎ้‡
Risk Class 2
Cancelled

Registration Details

2a7cf9c5952a6e4c0a5e5658cf5fc108

DHA00602170301

Company Information

Product Details

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

J General hospital and personal use equipment

J.5200 Endovascular catheters

import

Dates and Status

Nov 16, 2010

Nov 16, 2020

Aug 05, 2022

Cancellation Information

Logged out

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