CC Flex [Cobalt Chromium Coronary Stent System] - DRAP MDIR-0000183 (Class D)

DRAP REGISTERED MEDICAL DEVICE

CC Flex [Cobalt Chromium Coronary Stent System] is registered with DRAP under number MDIR-0000183 as a Class D (high risk) medical device, imported. The listed holder is Saving Life Technologies (SLT). Its listed renewal date (27 Feb 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-0000183 · 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 27 Feb 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-00053
DeviceCC Flex [Cobalt Chromium Coronary Stent System]
ClassD
Listed holderSaving Life Technologies (SLT)
Holder address427-K, Block Model Town, Lahore
Manufacturing siteM/s Eucatech AG Rebgartenweg 27, 79576 Weil am Rhein/ Germany.
Issued28 Feb 2019
Renewal date27 Feb 2024
LicenceELI-00053

Specifications

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Screened 6 Oct 2026, 21:26 (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.

MDIR-0000181Eucalimus [Sirolimus Eluting Coronary Stent System]Class D
MDIR-0000182Euca VI [PTCA Balloon Catheter]Class D

Similar devices from other companies

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

MDIR-0007040FLEXITRON COBALT-60 SYSTEMClass CAllmed Solutions
MDIR-0000215Cobalt Chromium Coronary Stents [CoFlexus] with Delivery System Rapid ExchangeClass D4S International

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.