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"Laika" Serki Path Staining Reagent Set (Unsterilized) - Taiwan Registration 50bbed71a1ba4217fae78bc711b0b485

Access comprehensive regulatory information for "Laika" Serki Path Staining Reagent Set (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 50bbed71a1ba4217fae78bc711b0b485 and manufactured by LEICA BIOSYSTEMS RICHMOND, INC.. The authorized representative in Taiwan is NAN HO-SHING 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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50bbed71a1ba4217fae78bc711b0b485
Registration Details
Taiwan FDA Registration: 50bbed71a1ba4217fae78bc711b0b485
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Device Details

"Laika" Serki Path Staining Reagent Set (Unsterilized)
TW: "่Šๅก" ็‘ŸๅŸบๅธ•ๆ€ ๆŸ“่‰ฒ่ฉฆๅŠ‘็ต„(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

50bbed71a1ba4217fae78bc711b0b485

DHA04401163001

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

Apr 25, 2012

Apr 25, 2017

Nov 04, 2019

Cancellation Information

Logged out

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