DRAP registered medical device · imported

POWERFLEX PRO PTA Balloon Dilatation Catheter

Class D (high risk) · MDIR-0000588 · Global Marketing Services

✓ DRAP status Renewal due Renewal date passed 16 Jul 2024

Screened against DRAP's published lists

DRAP REGISTERED MEDICAL DEVICE

POWERFLEX PRO PTA Balloon Dilatation Catheter is registered with DRAP under number MDIR-0000588 as a Class D (high risk) medical device, imported. The listed holder is Global Marketing Services. Its listed renewal date (16 Jul 2024) has passed, so ask the supplier for the renewal letter.

Screening result

Imported device, registered with DRAP as Class D (high risk)
MDIR-0000588 · 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 16 Jul 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-00109

Device	POWERFLEX PRO PTA Balloon Dilatation Catheter
Class	D
Listed holder	Global Marketing Services
Holder address	111-B, Hali Road, Westridge 1, Rawalpindi., Godown: Same as above
Manufacturing site	M/s Cordis Corporation 14201 N.W. 60th Ave. Miami Lakes, FL 33014 USA M/s Nitinol Devices & Components Costa Rica S.R.L. Coyol Free Zone, Building B14, B15, B25 El Coyol, Alajuela 2 01 02 Costa Rica
Issued	17 Jul 2019
Renewal date	16 Jul 2024
Licence	ELI-00109

Specifications

No supplier specifications yet.

Supplier of this device? Add specifications (free during launch)

Screened 7 Oct 2026, 06:06 (Pakistan time). A screening aid, not an official DRAP verification.

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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.