DRAP REGISTERED MEDICAL DEVICE
Philips Hemodynamic Application is registered with DRAP under number MDIR-0008354 as a Class C (moderate to high risk) medical device, imported. The listed holder is Matora Digionics Pvt Ltd. It is listed as valid until 19 Mar 2030.
Screening result
i
Number type: imported, registered (Class B, C or D)
MDIR-0008354
MDIR-0008354
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Found in DRAP's published list
DRAP registered Class B/C/D list, 28 Aug 2025
DRAP registered Class B/C/D list, 28 Aug 2025
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Listed valid until 19 Mar 2030
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Holder has a DRAP import licence on file
ELI-00083
ELI-00083
| Device | Philips Hemodynamic Application |
|---|---|
| Class | C |
| Listed holder | Matora Digionics Pvt Ltd |
| Holder address | 130-C, Scotch Corner Upper Mall, Lahore. |
| Manufacturing site | M/s Philips Medical Systems Nederland B.V Veenpluis 6 5684PC Best, Netherlands |
| Issued | 20 Mar 2025 |
| Renewal date | 19 Mar 2030 |
| Licence | ELI-00083 |
Specifications
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Screened 5 Oct 2026, 00:50 (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.
| MDIR-0000968 | FebriDx (Differential Diagnostic testing (Fingerstick blood sample) | Class B |
| MDIR-0008346 | Philips Azurion 3 M12 (Image guide Therapy System) | Class C |
| MDIR-0008347 | Philips Azurion 5 M12 | Class C |
| 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-0009772 | Philips Stent boost [001007] | Class C |
| MDIR-0009773 | Philips XperGuide [001006] | Class C |
| MDIR-0009774 | Philips Embo Guide [001012] | Class C |
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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.