DLP Double Lumen Aortic Root Cannula with Vent Line - DRAP MDIR-0004124 (Class D)

DRAP REGISTERED MEDICAL DEVICE

DLP Double Lumen Aortic Root Cannula with Vent Line (Cardioplegia Cannula) [30401- 30402] is registered with DRAP under number MDIR-0004124 as a Class D (high risk) medical device, imported. The listed holder is Medtronic Pakistan (Pvt) Ltd.. It is listed as valid until 22 Nov 2027.

Screening result

i
Imported device, registered with DRAP as Class D (high risk)
MDIR-0004124 · 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 22 Nov 2027
✓
Holder has a DRAP import licence on file
ELI-00273
DeviceDLP Double Lumen Aortic Root Cannula with Vent Line (Cardioplegia Cannula) [30401- 30402]
ClassD
Listed holderMedtronic Pakistan (Pvt) Ltd.
Holder addressOcean Tower, 21st Floor, Plot No.G-3, Khayaban-e-Iqbal, Block 09, Clifton, Karachi.
Manufacturing siteM/s Medtronic Inc. 710 Medtronic Parkway, Minneapolis, MN 55432, USA M/s. Medtronic Perfusion systems 7611 Northland Drive, Minneapolis, MN 55428, USA.
Issued23 Nov 2022
Renewal date22 Nov 2027
LicenceELI-00273

Specifications

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Screened 5 Oct 2026, 15:50 (Pakistan time). A screening aid, not an official DRAP verification.

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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.