DRAP REGISTERED MEDICAL DEVICE
iVascular xperience Coronary balloon dilatation catheter is registered with DRAP under number MDIR-0002839 as a Class D (high risk) medical device, imported. The listed holder is Novatek Pakistan. Its listed renewal date (8 Sep 2026) has passed, so ask the supplier for the renewal letter.
Screening result
MDIR-0002839 · the class is taken from DRAP's list for this number
DRAP registered Class B/C/D list, 28 Aug 2025
It may have been renewed after DRAP's last list. Ask the vendor for the renewal letter.
ELI-00454
| Device | iVascular xperience Coronary balloon dilatation catheter |
|---|---|
| Class | D |
| Listed holder | Novatek Pakistan |
| Holder address | P-20, 1st Floor, Office No.1, Channab Market, Susan Road, Madina Town, Faisalabad |
| Manufacturing site | M/s Life Vascular Devices Biotech S.L. Cami de Can Ubach, 11 (Pol. Ind. Les Fallulles) 08620 Sant Vicenc dels Horts (Barcelona-Spain) |
| Issued | 9 Sep 2021 |
| Renewal date | 8 Sep 2026 |
| Licence | ELI-00454 |
Specifications
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Screened 5 Oct 2026, 15:50 (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-0000976 | LivePace T20 (Pace T20) | Class C |
| MDIR-0000977 | LivePace T10 (Pace T10) | Class C |
| MDIR-0001217 | Life-Stat Cardiopulmonary Resuscitator Model: 1008MII | Class B |
| MDIR-0001485 | Meditech (Microvent Resuscitator) | Class B |
| MDIR-0002836 | iVascular Navitian Coronary micro catheter | Class D |
| MDIR-0002837 | iVascular Capturer Thrombus extraction catheter | Class D |
| MDIR-0002838 | iVascular NC xperience Coronary balloon dilatation catheter | Class D |
| MDIR-0003042 | iVASCULAR Paclitaxel eluting rapid exchange balloon dilatation catheter | Class D |
| MDIR-0003043 | Airocide Models: GCS-25 Air Purification System GCS-50 Air Purification System GCS-100 Air Purification System | Class B |
| MDIR-0007535 | Metronic Medicale S.r.I (CHELT) | Class C |
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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.