DRAP REGISTERED MEDICAL DEVICE
Pro Via TM Steerable Guidewires is registered with DRAP under number MDIR-0000148 as a Class D (high risk) medical device, imported. The listed holder is Medtronic Pakistan (Pvt) Ltd.. Its listed renewal date (26 Feb 2024) has passed, so ask the supplier for the renewal letter.
Screening result
MDIR-0000148 · 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 | Pro Via TM Steerable Guidewires |
|---|---|
| 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 CEA Global Dominicana S.R.L. Zona Franca Industrial San Pedro de Macoris, San Pedro de Macoris 80916, Dominican Republic M/s Medtronic Vascular 37A Cherry Hill Dr Danvers, MA 01923 USA |
| Issued | 27 Feb 2019 |
| Renewal date | 26 Feb 2024 |
| Licence | ELI-00273 |
Specifications
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Screened 6 Oct 2026, 19:27 (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-0005562 | NEUROSCOUT Steerable Guidewires Cardiac guidewire | Class D | Johnson & Johnson Pakistan (Pvt) Ltd |
| MDIR-0004567 | AGILITY Steerable Guidewires. (Cardiac Guidewire) | Class D | Johnson & Johnson Pakistan (Pvt) Ltd |
| MDIR-0000315 | ATW Steerable Guidewires | Class D | Global Marketing Services |
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.