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
MDIR-0004124 · the class is taken from DRAP's list for this number
DRAP registered Class B/C/D list, 28 Aug 2025
ELI-00273
| Device | DLP Double Lumen Aortic Root Cannula with Vent Line (Cardioplegia Cannula) [30401- 30402] |
|---|---|
| Class | D |
| Listed holder | Medtronic Pakistan (Pvt) Ltd. |
| Holder address | Ocean Tower, 21st Floor, Plot No.G-3, Khayaban-e-Iqbal, Block 09, Clifton, Karachi. |
| Manufacturing site | M/s Medtronic Inc. 710 Medtronic Parkway, Minneapolis, MN 55432, USA M/s. Medtronic Perfusion systems 7611 Northland Drive, Minneapolis, MN 55428, USA. |
| Issued | 23 Nov 2022 |
| Renewal date | 22 Nov 2027 |
| Licence | ELI-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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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.
