DRAP REGISTERED MEDICAL DEVICE
DLP Aortic Root Cannulae with Vent Line is registered with DRAP under number MDIR-0001010 as a Class D (high risk) medical device, imported. The listed holder is Medtronic Pakistan (Pvt) Ltd.. Its listed renewal date (9 Dec 2024) has passed, so ask the supplier for the renewal letter.
Screening result
MDIR-0001010
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 Aortic Root Cannulae with Vent Line |
|---|---|
| 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 (Minneapolis, MN 55447) 3800 Annapolis lane Minneapolis, MN USA M/s Medtronic Perfusion Systems 7611 Northland Dr Minneapolis, MN USA M/s Medtronic Mexico S. de R.L de CV Av. Paseo Cucapha 10510 EI lago Tijuana, Baja California C.P.22210 Mexico M/s Medplast Medical Inc 620 Watson SW GR MI 49504 USA |
| Issued | 10 Dec 2019 |
| Renewal date | 9 Dec 2024 |
| Licence | ELI-00273 |
Specifications
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Screened 5 Oct 2026, 12:34 (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.
| MDIR-0007587 | Cardioplegia circuit cannula (Aortic Root Cannula) | Class D | Microport Scientific Pakistan (Private) Limited |
| MDIR-0005968 | LivoNova Cardioplegia Cannula (Aortic root cannula) | Class D | Vertex Medical (Pvt) Ltd |
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| MDIR-0001609 | KANGXIN Extracorporeal Circuit auxiliary Cannulae (Aortic Root Cannulae) | Class D | Imtiaz Brothers |
| MDIR-0001517 | ANDOCOR Aortic Root Cannulae | Class D | Flowtronix Systems |
| MDIR-0000933 | SORIN Cardioplegia Aortic Root Cannulae | Class D | Pharma Consultant Pakistan (Pvt) Ltd |
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.