Taiwan FDA registration b4866e1ebf95a8b576f765e6bcd5e8fe

Rapid antibody medium

TW: 速銳快速抗體培養基
Taiwan flagTaiwan·Risk Class 1·CSL LIMITED·Registered Oct 29, 2010 – Oct 29, 2015Cancelled
Registration details
Analysis ID
b4866e1ebf95a8b576f765e6bcd5e8fe
Customs Code
DHA04400943001
Company information
Manufacturer
CSL LIMITED
Manufacturer Country
Australia
Authorized Representative
GIRAFFES PHARMACEUTICAL COMPANY LTD.
Product details
Intended Use
Limited to the first level identification range of intensive medium (B.9600) for in vitro diagnosis of medical device management methods.
Product Type (Level 1)
B Hematology, pathology, and genetics
Product Type (Level 2)
B.9600 Intensive medium for in vitro diagnostics
Import Information
import
Dates and status
Registration Date
Oct 29, 2010
Expiry Date
Oct 29, 2015
Cancellation Date
Apr 25, 2018
Cancellation information
Status
Logged out
Reason
自行鍵入
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About this record

Access comprehensive regulatory information for Rapid antibody medium in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b4866e1ebf95a8b576f765e6bcd5e8fe and manufactured by CSL LIMITED. The authorized representative in Taiwan is GIRAFFES PHARMACEUTICAL COMPANY LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including IMMULAB PTY LTD, and 1 recent registrations in the same category. 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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