DRAP registered medical device · imported

Angio-Seal VIP Vascular Closure Device AngioSeal VIP 610132 6Fr AngioSeal VIP 610133

Class D (high risk) · MDIR-0000244 · Intek Corporation

✓ DRAP status Renewal due Renewal date passed 3 Apr 2024
Screened against DRAP's published lists

DRAP REGISTERED MEDICAL DEVICE

Angio-Seal VIP Vascular Closure Device AngioSeal VIP 610132 6Fr AngioSeal VIP 610133 8Fr is registered with DRAP under number MDIR-0000244 as a Class D (high risk) medical device, imported. The listed holder is Intek Corporation. Its listed renewal date (3 Apr 2024) has passed, so ask the supplier for the renewal letter.

Screening result

i
Imported device, registered with DRAP as Class D (high risk)
MDIR-0000244 · 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
!
Renewal date passed on 3 Apr 2024
It may have been renewed after DRAP's last list. Ask the vendor for the renewal letter.
✓
Holder has a DRAP import licence on file
ELI-00034
DeviceAngio-Seal VIP Vascular Closure Device AngioSeal VIP 610132 6Fr AngioSeal VIP 610133 8Fr
ClassD
Listed holderIntek Corporation
Holder addressOffice No 30, First Floor Al Amin Plaza, The Mall Rawalpindi., Godown Address: 25 A Nagi Road Westridge 1, Rawalpindi.
Manufacturing siteM/s Terumo Medical Corporation 2101 Cottontail Lane Somerset, New Jersey 08873 USA M/s Terumo Puerto Rico, LLC Caguas West Industrial Park Lot 21-B Street Caguas, PR 00725, USA M/s St. Jude Medical 14901 Deveau Pl. Minnetonka, MN 55345 USA
Issued5 Mar 2019
Renewal date3 Apr 2024
LicenceELI-00034

Specifications

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Screened 7 Oct 2026, 02:03 (Pakistan time). A screening aid, not an official DRAP verification.

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MDIR-0000385MemoPart TM Occluder Delivery SystemClass D
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MDIR-0000387Figulla Flex II ASD OccluderClass D
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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.