DRAP registered medical device · imported

LivaNova Perfusion System Monitor Essenz Patient Monitor

Class B (low to moderate risk) · MDIR-0008215 · Vertex Medical (Pvt) Ltd

✓ DRAP status Listed Valid until 19 Mar 2030
Screened against DRAP's published lists

DRAP REGISTERED MEDICAL DEVICE

LivaNova Perfusion System Monitor Essenz Patient Monitor is registered with DRAP under number MDIR-0008215 as a Class B (low to moderate risk) medical device, imported. The listed holder is Vertex Medical (Pvt) Ltd. It is listed as valid until 19 Mar 2030.

Screening result

i
Imported device, registered with DRAP as Class B (low to moderate risk)
MDIR-0008215 · the class is taken from DRAP's list for this number
✓
Found in DRAP's published list
DRAP registered Class B/C/D list, 28 Aug 2025
✓
Listed valid until 19 Mar 2030
✓
Holder has a DRAP import licence on file
ELI-00150
DeviceLivaNova Perfusion System Monitor Essenz Patient Monitor
ClassB
Listed holderVertex Medical (Pvt) Ltd
Holder address401-402, Block-F, Johar Town, Lahore, Godown: Building No.13, Shadiwal, Johar Town, Lahore
Manufacturing siteM/s LivaNova Deutschland GmbH Lindberghstrasse. 25 80939 Munchen-Germany
Issued20 Mar 2025
Renewal date19 Mar 2030
LicenceELI-00150

Specifications

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Screened 7 Oct 2026, 05:19 (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.