Taiwan FDA registration 50bbed71a1ba4217fae78bc711b0b485

"Laika" Serki Path Staining Reagent Set (Unsterilized)

TW: "萊卡" 瑟基帕思染色試劑組(未滅菌)

Taiwan·Risk Class 1·LEICA BIOSYSTEMS RICHMOND, INC.·Registered Apr 25, 2012 – Apr 25, 2017Cancelled

Registration details

Analysis ID: 50bbed71a1ba4217fae78bc711b0b485
Customs Code: DHA04401163001

Company information

Manufacturer: LEICA BIOSYSTEMS RICHMOND, INC.
Manufacturer Country: United States
Authorized Representative: NAN HO-SHING CO., LTD.

Product details

Intended Use: Limited to the first grade identification range of dyes and chemical solution dyes (B.1850) of the management measures for medical devices.
Product Type (Level 1): B Hematology, pathology, and genetics
Product Type (Level 2): B.1850 Dyes and dyes for chemical solutions
Import Information: import

Dates and status

Registration Date: Apr 25, 2012
Expiry Date: Apr 25, 2017
Cancellation Date: Nov 04, 2019

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

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.