Eu Ivdd Eu Ivd General On The Market 🇩🇰 Denmark

SensiScreen

PentaBase A/S · 🇩🇰 Denmark
Devices (same UDI-DI)
1
Certificates
0
Countries
0
Notified Bodies
0

Basic Information

Primary DI
D-5713915SS002V5Q8
Basic UDI-DI Code
B-5713915SS002V5Q8
Reference
5525; 5530; 5535; 5336; 5341; 5346
Device Types
Single use
Regulation
Eu Ivdd
Classification
Eu Ivd General
Status
On The Market
Manufacturer
PentaBase A/S

Additional Description

SensiScreen® Liquid BRAF qPCR Assay is a semi-quantitative real-time Polymerase Chain Reaction (PCR) assay intended for the detection, identification, and relative quantification of specific somatic mutations in the human v-Raf murine sarcoma viral oncogene homolog B (BRAF) gene in cell-free DNA (cfDNA) purified from liquid biopsies including blood and plasma. The assay is used with real-time PCR systems and samples can be prepared using automated platforms or in manual workflows. The assay is an in vitro diagnostic medical device intended to aid in the detection, identification, monitoring of disease progression, and re-appearance based on BRAF mutation status. The test result correlates with the amount of BRAF mutant cfDNA. The results can be used to determine changes in BRAF mutation quantity levels in patients over time such as during cancer interventions and as an aid in selecting proper treatment for cancer. SensiScreen® Liquid BRAF qPCR Assay is intended to be used by healthcare professionals or qualified laboratory personnel instructed and trained in the techniques of real-time PCR as well as proficient in handling biological samples. Medical interventions based on results from this product requires medical authorization.

CND Nomenclature Codes

Code Description
W01060299 TESTS FOR ACQUIRED GENETIC OR CHROMOSOMAL ALTERATIONS - OTHER

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