Last synced on 30 May 2025 at 11:05 pm

Synthetic Next-Generation Sequencing Quality Control And Filler Material

Page Type
Product Code
Definition
A synthetic next-generation sequencing filler material which contains an adapter-ligated library which allows users to run partial batches of next-generation sequencing assays by adding the material to sample pools to fill in for incomplete batched runs.
Physical State
The reagent includes synthetic DNA sequences.
Technical Method
The material is a synthetic sequence material which can be added to sample pools immediately prior to loading the sequencer to allow sequencing runs to be processed that do not have a sufficient number of patient samples. The material may also be used to quality control sequencing metrics.
Target Area
Not applicable.
Review Panel
Pathology
Submission Type
Contact ODE
Device Classification
N
GMP Exempt?
No
Summary Malfunction Reporting
Ineligible
Implanted Device
No
Life-Sustain/Support Device
No
Third Party Review
Not Third Party Eligible

No Linked CFR Text

As product code QFI is assigned to devices that are "not-classified", it is not linked to any specific regulation and CFR section.

Synthetic Next-Generation Sequencing Quality Control And Filler Material

Page Type
Product Code
Definition
A synthetic next-generation sequencing filler material which contains an adapter-ligated library which allows users to run partial batches of next-generation sequencing assays by adding the material to sample pools to fill in for incomplete batched runs.
Physical State
The reagent includes synthetic DNA sequences.
Technical Method
The material is a synthetic sequence material which can be added to sample pools immediately prior to loading the sequencer to allow sequencing runs to be processed that do not have a sufficient number of patient samples. The material may also be used to quality control sequencing metrics.
Target Area
Not applicable.
Review Panel
Pathology
Submission Type
Contact ODE
Device Classification
N
GMP Exempt?
No
Summary Malfunction Reporting
Ineligible
Implanted Device
No
Life-Sustain/Support Device
No
Third Party Review
Not Third Party Eligible

No Linked CFR Text

As product code QFI is assigned to devices that are "not-classified", it is not linked to any specific regulation and CFR section.