DRAP REGISTERED MEDICAL DEVICE
LivaNova Arterial Cardiopulmonary Bypass Cannulae is registered with DRAP under number MDIR-0002914 as a Class D (high risk) medical device, imported. The listed holder is Vertex Medical (Pvt) Ltd. It is listed as valid until 20 Oct 2026.
Screening result
MDIR-0002914 · the class is taken from DRAP's list for this number
DRAP registered Class B/C/D list, 28 Aug 2025
ELI-00150
| Device | LivaNova Arterial Cardiopulmonary Bypass Cannulae |
|---|---|
| Class | D |
| Listed holder | Vertex Medical (Pvt) Ltd |
| Holder address | 70-B-1, Gulberg -III Lahore |
| Manufacturing site | M/s. LivaNova USA, Inc 14401 West 65th Way Arvada, CO 80004 USA. |
| Issued | 22 Oct 2021 |
| Renewal date | 20 Oct 2026 |
| Licence | ELI-00150 |
Specifications
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Screened 5 Oct 2026, 19:21 (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.
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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.