DRAP REGISTERED MEDICAL DEVICE
DLP Femoral Arterial Cannula. is registered with DRAP under number MDIR-0004679 as a Class D (high risk) medical device, imported. The listed holder is Medtronic Pakistan (Pvt) Ltd.. It is listed as valid until 13 Feb 2028.
Screening result
MDIR-0004679
DRAP registered Class B/C/D list, 28 Aug 2025
ELI-00273
| Device | DLP Femoral Arterial Cannula. |
|---|---|
| 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., Plot No. S1, Survey 231, Sector 2, Road No. 4000, Korangi Industrial Area, Karachi. |
| Manufacturing site | M/s Medtronic Inc. 710 Medtronic Pkwy Minneapolis, MN USA 55432 M/s Medtronic Perfusion Sysytems 7611 Northland Dr Minneapolis, MN USA 55428 M/s Medtronic Mexico S.de R.L. de CV Av. Paseo Cucupah 10510 El Lago Tijuana Baja California MEXICO C.P 22210 M/s Viant Medical Inc 620 WATSON SW GR MI USA 49504 (Contract Manufacturer) |
| Issued | 14 Feb 2023 |
| Renewal date | 13 Feb 2028 |
| Licence | ELI-00273 |
Specifications
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Screened 5 Oct 2026, 07:56 (Pakistan time). A screening aid, not an official DRAP verification.
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Similar devices from other companies
Same device type listed by other holders, useful when comparing suppliers.
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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.