Devyser CFTR 68
Fragment analysis-based kit that enables fast and reliable detection of cystic fibrosis-causing mutations, using a multi-ethnic panel of 68 CFTR mutations that achieves high detection rates while keeping the workload and costs to a minimum.
68
Detects 68 CFTR mutations, the polyT tract and associated number of TG repeats
Allele-specific detection
CE-IVD
Single end-to-end CE-IVD solution
The next generation is here!

Multi-ethnic panel
For laboratories looking to improve detection rate while keeping a simple and fast workflow, Devyser CFTR 68 is a streamlined, two-tube solution that maximizes the detection rate by including a multi-ethnic panel of 68 mutations frequently found in the European population. It does not require the use of additional population-specific kits.
Downloads
Instructions for use
Enter access code found in the lower right corner of the label on the kit box.

Certificates
Download a specific Batch Release Certificate (BRC) below.
Guidelines and handbooks (6)
Addendum to handbook Devyser SeqStudio allele-specific products 7-B908 v2023-03-30 (English)
489 kb pdf
Addendum to handbook Devyser VeritiPro allele-specific products 7-B906 v2023-03-31 (English)
82 kb pdf
Product information (1)
Software settings (6)
Safety data sheets (5)
Data tables (1)
Enter access code found in the lower right corner of the label on the kit box.

Download a specific Batch Release Certificate (BRC) below.
Addendum to handbook Devyser SeqStudio allele-specific products 7-B908 v2023-03-30 (English)
489 kb pdf
Addendum to handbook Devyser VeritiPro allele-specific products 7-B906 v2023-03-31 (English)
82 kb pdf
Addendum to IFU Devyser allele-specific products VeritiPro 7-B905 v2023-03-31 (English)
110 kb pdf
Addendum to IFU Devyser SeqStudio allele-specific products 7-B907 v2023-03-30 (English)
510 kb pdf
Product details
CE-IVD
Devyser CFTR 68
Detection of the following CFTR mutations: 711+ 1G>T, 2043delG, 1677delTA, W1282X, R1283M, K710X, 3849+10kbC>T, 2789+5G>A, M1101K, G85E, 3905insT, 1525-1G>A, 2184delA, 3659delC, N1303K, 2184insA, 1812-1G->A, CFTRdele2,3, 2143delT, Y569D, R1162X, A561E, S1251N, P67L, R1158X, 1609delCA, Q493X, E60X, 1898+1G>A, 1898+5G>T, I507del, F508del, V520F, 394delTT, D1152H, V232D, L218X, 621+2T>C, 1717-1G>A, L206W, E92X, 3120+1G>A, G542X, S549N, G551D, 712-1G>T, R553X, 3272-26A>G, R560T, 2183AA>G, R117H, R117C, 1811+1.6kbA>G, 2869insG, Y122X, Q890X, R1066C, R347H, R347P, 1161delC, 1154ins TC, E92K, I336K, R334W, Y1092X (C>A), 621+1G>T, 1078delT, A455E and corresponding wildtype alleles. IVS8: 5T (including identification of TG9-13), 7T, 9T. Calibrated with G5.
8-A045-8
8-A045-24
8-A045-
Pack size: 8
Pack size: 24
Pack size: 48
RUO
Devyser CFTR 68
Detection of the following CFTR mutations: 711+ 1G>T, 2043delG, 1677delTA, W1282X, R1283M, K710X, 3849+10kbC>T, 2789+5G>A, M1101K, G85E, 3905insT, 1525-1G>A, 2184delA, 3659delC, N1303K, 2184insA, 1812-1G->A, CFTRdele2,3, 2143delT, Y569D, R1162X, A561E, S1251N, P67L, R1158X, 1609delCA, Q493X, E60X, 1898+1G>A, 1898+5G>T, I507del, F508del, V520F, 394delTT, D1152H, V232D, L218X, 621+2T>C, 1717-1G>A, L206W, E92X, 3120+1G>A, G542X, S549N, G551D, 712-1G>T, R553X, 3272-26A>G, R560T, 2183AA>G, R117H, R117C, 1811+1.6kbA>G, 2869insG, Y122X, Q890X, R1066C, R347H, R347P, 1161delC, 1154ins TC, E92K, I336K, R334W, Y1092X (C>A), 621+1G>T, 1078delT, A455E and corresponding wildtype alleles. IVS8: 5T (including identification of TG9-13), 7T, 9T. Calibrated with G5.
8-A403-8
8-A403-24
8-A403-
Pack size: 8
Pack size: 24
Pack size: 48
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