DRAP REGISTERED MEDICAL DEVICE
DLP Femoral Arterial Cannula (Cardiopulmonary bypass cannula, arterial is registered with DRAP under number MDIR-0001331 as a Class D (high risk) medical device, imported. The listed holder is Medtronic Pakistan (Pvt) Ltd.. Its listed renewal date (17 Feb 2025) has passed, so ask the supplier for the renewal letter.
Screening result
MDIR-0001331
DRAP registered Class B/C/D list, 28 Aug 2025
It may have been renewed after DRAP's last list. Ask the vendor for the renewal letter.
ELI-00273
| Device | DLP Femoral Arterial Cannula (Cardiopulmonary bypass cannula, arterial |
|---|---|
| Class | D |
| Listed holder | Medtronic Pakistan (Pvt) Ltd. |
| Holder address | Office No. 1301, 13th Floor Dilkusha Forum Tariq Road, 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 55432 USA M/s Medtronic Perfusion Systems 7611 Northland Dr Minneapolis, MN 55428 USA |
| Issued | 18 Feb 2020 |
| Renewal date | 17 Feb 2025 |
| Licence | ELI-00273 |
Specifications
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Screened 5 Oct 2026, 04:04 (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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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.