Taiwan FDA registration 60cb0886af5714f72dc206dca8a3edef

Beiersda photoimmunoassay respiratory fusion virus assay reagent

TW: 拜爾斯達光學免疫法呼吸道融合病毒測定試劑

Taiwan·Risk Class 1·THERMO ELECTRON CORPORATION·Registered Nov 16, 2005 – Nov 16, 2010Cancelled

Registration details

Analysis ID: 60cb0886af5714f72dc206dca8a3edef
Customs Code: DHA04400197105

Company information

Manufacturer: THERMO ELECTRON CORPORATION
Manufacturer Country: United States
Authorized Representative: DITECH ENTERPRISE CO., LTD.

Product details

Intended Use: Detection of antibodies to respiratory fusion virus (nucleoproteins and fusion proteins) in nasal irrigation fluids and nasopharyngeal swab specimens.
Product Type (Level 1): C Immunology and microbiology
Import Information: import

Dates and status

Registration Date: Nov 16, 2005
Expiry Date: Nov 16, 2010
Cancellation Date: Nov 19, 2012

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for Beiersda photoimmunoassay respiratory fusion virus assay reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 60cb0886af5714f72dc206dca8a3edef and manufactured by THERMO ELECTRON CORPORATION. The authorized representative in Taiwan is DITECH ENTERPRISE 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.