X.ACT Carotid Stent System - DRAP MDIR-0003385 (Class D)

DRAP REGISTERED MEDICAL DEVICE

X.ACT Carotid Stent System is registered with DRAP under number MDIR-0003385 as a Class D (high risk) medical device, imported. The listed holder is Digital Imaging Systems. It is listed as valid until 17 May 2027.

Screening result

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Number type: imported, registered (Class B, C or D)
MDIR-0003385
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Found in DRAP's published list
DRAP registered Class B/C/D list, 28 Aug 2025
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Listed valid until 17 May 2027
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Holder has a DRAP import licence on file
ELI-00094
DeviceX.ACT Carotid Stent System
ClassD
Listed holderDigital Imaging Systems
Holder address121- Habitat Apartments, Shadman II, Ghaus-ul-Azam Road, Lahore
Manufacturing siteM/s Abbott Vascular 3200 Lakeside Drive, Santa Clara, California, 95054, USA M/s Abbott Vascular 26531 Ynez Road Temecula, California 92591, USA
Issued18 May 2022
Renewal date17 May 2027
LicenceELI-00094

Specifications

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Screened 5 Oct 2026, 11:39 (Pakistan time). A screening aid, not an official DRAP verification.

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MDIR-0000016Hi-Torque Whisper Guide Wire with Hydrophilic CoatingClass D
MDIR-0000017Hi-Torque Balance Middle Weight Guide WireClass D

Similar devices from other companies

Same device type listed by other holders, useful when comparing suppliers.

MDIR-0000393CASPER TM RX Carotid Artery Stent SystemClass DIntek Corporation
MDIR-0000093Carotid Wallstent TM Monorail TM Closed Cell Self-Expanding StentClass DFerozsons Laboratories Limited

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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.