VexPander Coronary Dilatation Balloon Catheter - DRAP MDIR-0007163 (Class D)

DRAP REGISTERED MEDICAL DEVICE

VexPander Coronary Dilatation Balloon Catheter (Non-compliant) is registered with DRAP under number MDIR-0007163 as a Class D (high risk) medical device, imported. The listed holder is The Cure. It is listed as valid until 15 Sep 2029.

Screening result

i
Number type: imported, registered (Class B, C or D)
MDIR-0007163
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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 15 Sep 2029
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Holder has a DRAP import licence on file
ELI-00567
DeviceVexPander Coronary Dilatation Balloon Catheter (Non-compliant)
ClassD
Listed holderThe Cure
Holder address1st Floor, Office No. 6, Capri Center, Firdous Market, Gulberg III, Lahore
Manufacturing siteM/s Dongguan TT Medical, Inc. Building No. 1, 1 Taoyuan Road, Songshan Lake National High-Tech Industrial Park, Dongguan, Guangdong, PR China 523808
Issued16 Sep 2024
Renewal date15 Sep 2029
LicenceELI-00567

Specifications

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Screened 5 Oct 2026, 09:27 (Pakistan time). A screening aid, not an official DRAP verification.

More devices from this holder

Other DRAP registrations and enlistments listed for the same company.

MDIE-0000665Wellex ManifoldClass A
MDIR-0005043Wellex Diagnostic CathetersClass B
MDIR-0005044WellexIntroducer Sheath SetsClass B
MDIR-0005045Wellex Hemostatis valvesClass B
MDIR-0005046Wellex Inflation DeviceClass B
MDIR-0005047Wellex Introducer NeedlesClass B
MDIR-0005048Wellex Guide WiresClass B
MDIR-0005403Wellex Guiding CathetersClass D
MDIR-0005623DIANOVA (Dialysis machine)Class C
MDIR-0005825DIADISINFECT (Hemodialysis machine disinfectant)Class C
MDIR-0006557DIADISINFECT Plus (Hemodialysis machine disinfectant) [DIADISINFECT Plus-5 DIADISINFECT Plus -10]Class C
MDIR-0007161VesPenetrator Coronary Dilatation Balloon Catheter (CTO)Class D

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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.