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Hannitec blood bag tube sealer (unsterilized) - Taiwan Registration 7ba011335eaeb5c7b518c21ced0bbe8c

Access comprehensive regulatory information for Hannitec blood bag tube sealer (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 7ba011335eaeb5c7b518c21ced0bbe8c and manufactured by HAEMONETICS CORPORATION. The authorized representative in Taiwan is HAEMONETICS ASIA INCORPORATED TAIWAN BRANCH (U.S.A.).

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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7ba011335eaeb5c7b518c21ced0bbe8c
Registration Details
Taiwan FDA Registration: 7ba011335eaeb5c7b518c21ced0bbe8c
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Device Details

Hannitec blood bag tube sealer (unsterilized)
TW: โ€œๆผขๅฐผๅธๅ…‹โ€่ก€่ข‹็ฎกๅฐๅฃๆฉŸ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

7ba011335eaeb5c7b518c21ced0bbe8c

DHA04400831302

Company Information

United States

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Equipment "Heating and Sealing Equipment (B.9750)".

B Hematology, pathology, and genetics

B.9750 Heat-sealing equipment

import

Dates and Status

Nov 23, 2009

Nov 23, 2019

Jun 16, 2022

Cancellation Information

Logged out

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