DRAP REGISTERED MEDICAL DEVICE
Confida Brecker Guidewire GWBC30 (Cardiac/peripheral vascular guidewire, single-use) is registered with DRAP under number MDIR-0001024 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-0001024
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 | Confida Brecker Guidewire GWBC30 (Cardiac/peripheral vascular guidewire, single-use) |
|---|---|
| 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 Heart Valves Division 1851 East Deere Ave. Santa Ana, CA USA 92705 M/s Epflex feinwerktechnik GmbH IM Schwoellbogen 24 Dettingen/Erms, Baden-wurttemberg 72581 Germany |
| Issued | 10 Dec 2019 |
| Renewal date | 9 Dec 2024 |
| Licence | ELI-00273 |
Specifications
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Screened 5 Oct 2026, 06:42 (Pakistan time). A screening aid, not an official DRAP verification.
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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.