PUREFLEX Arterial Cannula
Class D (high risk) · MDIR-0003900 · Vertex Medical (Pvt) Ltd
DRAP REGISTERED MEDICAL DEVICE
PUREFLEX Arterial Cannula (Cardiopulmonary bypass cannula, arterial) is registered with DRAP under number MDIR-0003900 as a Class D (high risk) medical device, imported. The listed holder is Vertex Medical (Pvt) Ltd. It is listed as valid until 30 Oct 2027.
Screening result
MDIR-0003900 · the class is taken from DRAP's list for this number
DRAP registered Class B/C/D list, 28 Aug 2025
ELI-00150
| Device | PUREFLEX Arterial Cannula (Cardiopulmonary bypass cannula, arterial) |
|---|---|
| Class | D |
| Listed holder | Vertex Medical (Pvt) Ltd |
| Holder address | 70-B-1, Gulberg -III Lahore |
| Manufacturing site | M/s Sorin Group Italia S.r.L Via Statale Nord 12, 86 41037 Mirandola MO, Italy |
| Issued | 31 Oct 2022 |
| Renewal date | 30 Oct 2027 |
| Licence | ELI-00150 |
Specifications
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Screened 7 Oct 2026, 08:01 (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.