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Helen Na Interface Fluid - Taiwan Registration 65f75fd909a881e6b853f71077c28399

Access comprehensive regulatory information for Helen Na Interface Fluid in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 65f75fd909a881e6b853f71077c28399 and manufactured by HELENA LABORATORIES, INC.. The authorized representative in Taiwan is SHANG LI INSTRUMENTS CO., LTD..

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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65f75fd909a881e6b853f71077c28399
Registration Details
Taiwan FDA Registration: 65f75fd909a881e6b853f71077c28399
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Device Details

Helen Na Interface Fluid
TW: ๆตทๅ€ซ้‚ฃ็•Œ้ขๆถฒ
Risk Class 1
Cancelled

Registration Details

65f75fd909a881e6b853f71077c28399

DHA04400110703

Company Information

United States

Product Details

The interfacial conductive fluid for the electrophoresis tank.

B Hematology, pathology, and genetics

B.4010 Reaction Reagents for General Purposes

import

Dates and Status

Oct 20, 2005

Oct 20, 2015

Jul 31, 2018

Cancellation Information

Logged out

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