Taiwan FDA registration 20792bd81fb98f913f85c2a0e1673cc1

Aifa type A streptococcus rapid assay reagent

TW: 愛喜發A型鏈球菌快速測定試劑

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

Registration details

Analysis ID: 20792bd81fb98f913f85c2a0e1673cc1
Customs Code: DHA04400196102

Company information

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

Product details

Intended Use: Qualitative detection of group A streptococcal antigen in throat swab specimens or as a reagent to confirm group A streptococcal colonies in bacterial culture.
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 Aifa type A streptococcus rapid 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 20792bd81fb98f913f85c2a0e1673cc1 and manufactured by THERMO ELECTRON CORPORATION. The authorized representative in Taiwan is DITECH ENTERPRISE CO., LTD..

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