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"TAI TSANG" TUBE SEALER (NON-STERILE) - Taiwan Registration 2592c2a8b12ec673fbbb1f290600ddd0

Access comprehensive regulatory information for "TAI TSANG" TUBE SEALER (NON-STERILE) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2592c2a8b12ec673fbbb1f290600ddd0 and manufactured by LJUNGBERG & KOGEL AB. The authorized representative in Taiwan is TAI TSANG TECHNOLOGY CORP..

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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2592c2a8b12ec673fbbb1f290600ddd0
Registration Details
Taiwan FDA Registration: 2592c2a8b12ec673fbbb1f290600ddd0
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Device Details

"TAI TSANG" TUBE SEALER (NON-STERILE)
TW: "ๆณฐ็‘ฒ" ่ก€่ข‹ๅฐๅฃๆฉŸ (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

2592c2a8b12ec673fbbb1f290600ddd0

Ministry of Health Medical Device Import No. 015223

DHA09401522301

Company Information

Sweden

Product Details

B Hematology and pathology devices

B9750 Heat sealing equipment

Imported from abroad

Dates and Status

May 15, 2015

May 15, 2020

Aug 05, 2022

Cancellation Information

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