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"Leica" Serki Path staining kit (unsterilized) - Taiwan Registration 496f1a9f083864283dff341809356736

Access comprehensive regulatory information for "Leica" Serki Path staining kit (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 496f1a9f083864283dff341809356736 and manufactured by LEICA BIOSYSTEMS RICHMOND INC.. The authorized representative in Taiwan is BOND BIOTECH, INC..

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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496f1a9f083864283dff341809356736
Registration Details
Taiwan FDA Registration: 496f1a9f083864283dff341809356736
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Device Details

"Leica" Serki Path staining kit (unsterilized)
TW: "ๅพ ๅก"็‘ŸๅŸบๅธ•ๆ€ๆŸ“่‰ฒ่ฉฆๅŠ‘็ต„(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

496f1a9f083864283dff341809356736

DHA04401045807

Company Information

United States

Product Details

Limited to the first grade identification range of dyes and chemical solution dyes (B.1850) of the management measures for medical devices.

B Hematology, pathology, and genetics

B.1850 Dyes and dyes for chemical solutions

import

Dates and Status

Jun 09, 2011

Jun 09, 2026

Sep 30, 2021

Cancellation Information

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