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"Leica" Surgipath Stains Reagent Kit (Non-Sterile) - Taiwan Registration 50180a08483144a3d08c4473ece6499b

Access comprehensive regulatory information for "Leica" Surgipath Stains Reagent Kit (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 50180a08483144a3d08c4473ece6499b 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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50180a08483144a3d08c4473ece6499b
Registration Details
Taiwan FDA Registration: 50180a08483144a3d08c4473ece6499b
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Device Details

"Leica" Surgipath Stains Reagent Kit (Non-Sterile)
TW: "ๅพ ๅก"็‘ŸๅŸบๅธ•ๆ€ๆŸ“่‰ฒ่ฉฆๅŠ‘็ต„(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

50180a08483144a3d08c4473ece6499b

Ministry of Health Medical Device Import Registration No. 010458

DHA08401045804

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 and pathology devices

B1850 Dyes and chemical solution dyes

Imported from abroad

Dates and Status

Oct 01, 2021

Oct 31, 2026