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"Kemel" drug sealed closed infusion sleeve - Taiwan Registration 0ffadcbc7a6811fa999fb17e19ae711f

Access comprehensive regulatory information for "Kemel" drug sealed closed infusion sleeve in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0ffadcbc7a6811fa999fb17e19ae711f and manufactured by CARMEL PHARMA AB. The authorized representative in Taiwan is MEDFRONT MEDICAL TECHNOLOGY CORPORATION.

This page provides complete technical specifications, regulatory compliance details. 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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0ffadcbc7a6811fa999fb17e19ae711f
Registration Details
Taiwan FDA Registration: 0ffadcbc7a6811fa999fb17e19ae711f
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Device Details

"Kemel" drug sealed closed infusion sleeve
TW: โ€œๅฏ็พŽ็ˆพโ€่—ฅๅฐๅฏ†้–‰ๅผ่ผธๆถฒๅฅ—
Risk Class 2
Cancelled

Registration Details

0ffadcbc7a6811fa999fb17e19ae711f

DHA00602106100

Company Information

Sweden

Product Details

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

J General hospital and personal use equipment

J.5440 ่ก€็ฎกๅ…ง่ผธๆถฒๅฅ—

import

Dates and Status

May 27, 2010

May 27, 2015

Jul 02, 2018

Cancellation Information

Logged out

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