DRAP REGISTERED MEDICAL DEVICE
ANDOCOR Aortic Root Cannulae is registered with DRAP under number MDIR-0001517 as a Class D (high risk) medical device, imported. The listed holder is Flowtronix Systems. Its listed renewal date (8 Jun 2025) has passed, so ask the supplier for the renewal letter.
Screening result
MDIR-0001517
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.
That list covers manually issued licences only. Ask for a copy of the establishment licence.
| Device | ANDOCOR Aortic Root Cannulae |
|---|---|
| Class | D |
| Listed holder | Flowtronix Systems |
| Holder address | Flat No. 02, 1st Floor Al-Ashraf Plaza, Range Road, Rawalpindi |
| Manufacturing site | M/s Andocor NV Kwikaard 104 -2980 Zoersel- Belgium |
| Issued | 9 Jun 2020 |
| Renewal date | 8 Jun 2025 |
Specifications
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Screened 5 Oct 2026, 01:08 (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-0002001 | Hemonart Compact One 9 ACT Analyzer | Class A |
| MDIR-0001065 | ABLE (Disposable Fistula Needles) | Class B |
| MDIR-0001066 | ABLE (Disposable Haemodialysers) | Class C |
| MDIR-0001067 | ABLE (Central Venous Catheter Kit). | Class D |
| MDIR-0001068 | ANDOCOR Cardiopleagia Sets | Class D |
| MDIR-0001069 | ANDOCOR Pericardial Sump | Class B |
| MDIR-0001070 | ANDOCOR Ostial Perfusion Cannulae | Class D |
| MDIR-0001071 | ANDOCOR Silicone Vent Catheter | Class D |
| MDIR-0001072 | ANDOCOR (Vessel Cannula with closed back check valve) | Class B |
| MDIR-0001073 | ANDOCOR Cannulation Torniquet Set | Class B |
| MDIR-0001074 | IBC Aortic Punch | Class B |
| MDIR-0001075 | ABLE (Disposable Blood Lines) | Class B |
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.