Philips Azurion 5 M20 - DRAP MDIR-0008348 (Class C)

DRAP REGISTERED MEDICAL DEVICE

Philips Azurion 5 M20 is registered with DRAP under number MDIR-0008348 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
Imported device, registered with DRAP as Class C (moderate to high risk)
MDIR-0008348 · the class is taken from DRAP's list for this number
✓
Found in DRAP's published list
DRAP registered Class B/C/D list, 28 Aug 2025
✓
Listed valid until 19 Mar 2030
✓
Holder has a DRAP import licence on file
ELI-00083
DevicePhilips Azurion 5 M20
ClassC
Listed holderMatora Digionics Pvt Ltd
Holder address130-C, Scotch Corner Upper Mall, Lahore.
Manufacturing siteM/s Philips Medical Systems Nederland B.V Veenpluis 6 5684PC Best, Netherlands
Issued20 Mar 2025
Renewal date19 Mar 2030
LicenceELI-00083

Specifications

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Screened 5 Oct 2026, 13:20 (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-0000968FebriDx (Differential Diagnostic testing (Fingerstick blood sample)Class B
MDIR-0008346Philips Azurion 3 M12 (Image guide Therapy System)Class C
MDIR-0008347Philips Azurion 5 M12Class C
MDIR-0008349Philips Azurion 7 B12Class C
MDIR-0008350Philips Azurion 3 M15Class C
MDIR-0008351Philips Azurion 7 M12Class C
MDIR-0008352Philips Azurion 7 M20Class C
MDIR-0008353Philips Azurion 7 B20Class C
MDIR-0008354Philips Hemodynamic ApplicationClass C
MDIR-0009772Philips Stent boost [001007]Class C
MDIR-0009773Philips XperGuide [001006]Class C
MDIR-0009774Philips 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.