DRAP REGISTERED MEDICAL DEVICE
Resolute Onyx Zotarolimus-Eluting Coronary Stent System is registered with DRAP under number MDIR-0000581 as a Class D (high risk) medical device, imported. The listed holder is Medtronic Pakistan (Pvt) Ltd.. Its listed renewal date (16 Jul 2024) has passed, so ask the supplier for the renewal letter.
Screening result
MDIR-0000581 · the class is taken from DRAP's list for this number
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 | Resolute Onyx Zotarolimus-Eluting Coronary Stent System |
|---|---|
| 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 Parkway NE, Minneapolis MN 55432, USA M/s Medtronic Ireland Parkmore Business Park West Galway, Ireland |
| Issued | 17 Jul 2019 |
| Renewal date | 16 Jul 2024 |
| Licence | ELI-00273 |
Specifications
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Screened 5 Oct 2026, 14:17 (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.