Taiwan FDA registration bf2b47b2f47827db0c2e9c15fb7cd879

BECKMAN COULTER COULTER LH SERIES RETIC PAK (Non-Sterile)

TW: 貝克曼庫爾特庫爾特LH系列網狀紅血球處理液 (未滅菌)

Taiwan·Risk Class 1·MD·BECKMAN COULTER INC.·Registered Oct 01, 2021 – Oct 31, 2025Expired

Registration details

Analysis ID: bf2b47b2f47827db0c2e9c15fb7cd879
License Form: Ministry of Health Medical Device Import Registration No. 000212
Customs Code: DHA08400021205

Company information

Manufacturer: BECKMAN COULTER INC.
Manufacturer Country: United States
Authorized Representative: BECKMAN COULTER TAIWAN INC., TAIWAN BRANCH (U.S.A.)

Product details

Intended Use: Used in the Coulter GEN.STM and LH750 blood analyzers for the removal of hemoglobin from red blood cells and reticular red blood cell staining.
Product Type (Level 1): B Hematology and pathology devices
Product Type (Level 2): B1850 Dyes and chemical solution dyes
Import Information: Imported from abroad

Dates and status

Registration Date: Oct 01, 2021
Expiry Date: Oct 31, 2025

About this record

Access comprehensive regulatory information for BECKMAN COULTER COULTER LH SERIES RETIC PAK (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 bf2b47b2f47827db0c2e9c15fb7cd879 and manufactured by BECKMAN COULTER INC.. The authorized representative in Taiwan is BECKMAN COULTER TAIWAN INC., TAIWAN BRANCH (U.S.A.).

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