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Classified as US Food and Drug Administration Class I Medical Device for in vitro diagnostic use
Conforms to IVDD (98⁄79⁄EC) requirements and labeled in Europe with a CE IVD mark
Manufactured to ISO 13485 and Gmp requirements
Cat Number: STEM-PEPO-0028-ZJF
Application: For real-time PCR (qPCR)
Model: Veriti Dx