DRAP REGISTERED MEDICAL DEVICE
FebriDx (Differential Diagnostic testing (Fingerstick blood sample) is registered with DRAP under number MDIR-0000968 as a Class B (low to moderate risk) medical device, imported. The listed holder is Matora Digionics Pvt Ltd. Its listed renewal date (2 Dec 2024) has passed, so ask the supplier for the renewal letter.
Screening result
MDIR-0000968 · the class is taken from DRAP's list for this number
DRAP registered Class B/C/D list, 28 Aug 2025
It may have been renewed after DRAP's last list. Ask the vendor for the renewal letter.
ELI-00083
| Device | FebriDx (Differential Diagnostic testing (Fingerstick blood sample) |
|---|---|
| Class | B |
| Listed holder | Matora Digionics Pvt Ltd |
| Holder address | 130-C, Scotch Corner Upper Mall, Lahore. |
| Manufacturing site | M/s Rapid Pathogen Screening Inc Screening 7227 Dlainey Court Sarasota, FL USA 34240 |
| Issued | 3 Dec 2019 |
| Renewal date | 2 Dec 2024 |
| Licence | ELI-00083 |
Specifications
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Screened 6 Oct 2026, 18:36 (Pakistan time). A screening aid, not an official DRAP verification.
More devices from this holder
Other DRAP registrations and enlistments listed for the same company.
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| MDIR-0008348 | Philips Azurion 5 M20 | Class C |
| MDIR-0008349 | Philips Azurion 7 B12 | Class C |
| MDIR-0008350 | Philips Azurion 3 M15 | Class C |
| MDIR-0008351 | Philips Azurion 7 M12 | Class C |
| MDIR-0008352 | Philips Azurion 7 M20 | Class C |
| MDIR-0008353 | Philips Azurion 7 B20 | Class C |
| MDIR-0008354 | Philips Hemodynamic Application | Class C |
| MDIR-0009772 | Philips Stent boost [001007] | Class C |
| MDIR-0009773 | Philips XperGuide [001006] | Class C |
| MDIR-0009774 | Philips Embo Guide [001012] | Class C |
Corrections
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Source: DRAP's published provisional lists. A screening aid, not an official DRAP verification; confirm with DRAP and the supplier's original documents.
