BeGraft Coronary Stent Graft System - DRAP MDIR-0001494 (Class D)

DRAP REGISTERED MEDICAL DEVICE

BeGraft Coronary Stent Graft System is registered with DRAP under number MDIR-0001494 as a Class D (high risk) medical device, imported. The listed holder is Verizon. Its listed renewal date (17 May 2025) has passed, so ask the supplier for the renewal letter.

Screening result

i
Number type: imported, registered (Class B, C or D)
MDIR-0001494
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Found in DRAP's published list
DRAP registered Class B/C/D list, 28 Aug 2025
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Renewal date passed on 17 May 2025
It may have been renewed after DRAP's last list. Ask the vendor for the renewal letter.
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Holder has a DRAP import licence on file
ELI-00087
DeviceBeGraft Coronary Stent Graft System
ClassD
Listed holderVerizon
Holder address60-D F.C.C Zahoor Elahi Road Gulberg- IV, Lahore.
Manufacturing siteM/s Bentley InnoMed GmbH Lotzenacker 25 72379 Hechingen,Germany
Issued18 May 2020
Renewal date17 May 2025
LicenceELI-00087

Specifications

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Screened 5 Oct 2026, 12:33 (Pakistan time). A screening aid, not an official DRAP verification.

More devices from this holder

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MDIR-0000233St. Jude Medical Tissue Valve Trifecta TM Valve Aortic Sizes 19mm-29mmClass D
MDIR-0000234SJM Masters HP Valved Graft with Gelweave Valsalva TM TechnologyClass D
MDIR-0000235St. Jude Medical Mechanical Heart Valve-SJM Master Series (Rotatable) Aortic Hemodynamic PlusClass D
MDIR-0000236St. Jude Medical Mechanical Heart Valve-SJM Master Series (Rotatable) Aortic Expanded Hemodynamic PlusClass D

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.