†The LigaSure™ XP Maryland jaw device is indicated for use in general surgery and such surgical specialties as colorectal, bariatric, urologic, vascular, thoracic, and gynecologic.
‡Compared to their current preferred device; 21 of 23 surgeons agreed during clinical procedures.
§Thick tissue is defined as nondissected vascular tissue or fatty tissue.
Ω29 out of 29 surgeons agree.
††Bench tissue may not be indicative of clinical tissue performance
‡‡Compared to legacy LigaSure™ devices.
§§30 out of 30 surgeons agree.
ΩΩ24 out of 29 surgeons agree.
†††Compared to their current preferred device; 20 of 23 surgeons agreed during clinical procedures.
‡‡‡28 out of 29 surgeons agree.
§§§15 out of 15 surgeons agree.
ΩΩΩ14 out of 14 surgeons agree.
1. Based on internal report #RE00457416 Rev A, Product introduction report: LigaSure™ XP Maryland jaw sealer/divider. May 2023.
2. Based on COGNOS and historical sales data, FY01–FY20. October 2019.
3. Based on internal report #RE00376094 Rev A, LigaSure™ XP Maryland jaw sealer/divider surgeon validation marketing report. Dec. 7–9 and 14–16, 2021.
4. Based on internal report #RE00442444 Rev A, Comparison of the renal artery bench bundle burst pressure performance with the LigaSure™ XP Maryland jaw sealer/divider, Voyant™* Maryland Fusion, Enseal™* X1 curved jaw, and LigaSure™ LF19XX devices. Jan. 23, 2023.
5. Based on internal report #RE00372649 Rev A, Archer surgeon summative evaluation report. March 22, 2022.
6. Based on internal report #RE00415591 Rev. A, LIG-48 LMXJXXX Archer BOE — jaw seal plate texture grip strength.
7. Based on internal report #RE00370099 Rev A, Verification of LigaSure™ XP Maryland jaw sealer/divider in a bench burst study burst test. March 30, 2022.
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