Taiwan FDA registration 5f3c2e61e4f82b51a6ba2001dafe98e9

Hypertherm Respiratory Virus Screening and Identification Kit (Unsterilized)

TW: 海柏呼吸道病毒篩選和鑑定試劑組(未滅菌)

Taiwan·Risk Class 1·DIAGNOSTIC HYBRIDS INCORPORATION·Registered Oct 08, 2009 – Oct 08, 2024Expired

Registration details

Analysis ID: 5f3c2e61e4f82b51a6ba2001dafe98e9
Customs Code: DHA04400819101

Company information

Manufacturer: DIAGNOSTIC HYBRIDS INCORPORATION
Manufacturer Country: United States
Authorized Representative: GLOWAY CO., LTD.

Product details

Intended Use: Limited to the classification and grading management of medical devices, the first level identification range of "respiratory fusion cell virus serum reagent (C.3480)".
Product Type (Level 1): C Immunology and microbiology
Product Type (Level 2): C.3480 呼吸道融合細胞病毒血清試劑
Import Information: import

Dates and status

Registration Date: Oct 08, 2009
Expiry Date: Oct 08, 2024

About this record

Access comprehensive regulatory information for Hypertherm Respiratory Virus Screening and Identification Kit (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5f3c2e61e4f82b51a6ba2001dafe98e9 and manufactured by DIAGNOSTIC HYBRIDS INCORPORATION. The authorized representative in Taiwan is GLOWAY CO., LTD..

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