Renamic Neo
Class D (high risk) · MDIR-0006111 · Flowtronix Systems
DRAP REGISTERED MEDICAL DEVICE
Renamic Neo (Programming Device and its external components) is registered with DRAP under number MDIR-0006111 as a Class D (high risk) medical device, imported. The listed holder is Flowtronix Systems. It is listed as valid until 28 Apr 2029.
Screening result
MDIR-0006111 · the class is taken from DRAP's list for this number
DRAP registered Class B/C/D list, 28 Aug 2025
That list covers manually issued licences only. Ask for a copy of the establishment licence.
| Device | Renamic Neo (Programming Device and its external components) |
|---|---|
| Class | D |
| Listed holder | Flowtronix Systems |
| Holder address | Flat No. 02, 1st Floor Al-Ashraf Plaza, Range Road, Rawalpindi |
| Manufacturing site | M/s Biotronik SE & Co. KG Woermannkehre 1, 12359 Berlin, Germany |
| Issued | 29 Apr 2024 |
| Renewal date | 28 Apr 2029 |
Specifications
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Screened 7 Oct 2026, 03:22 (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 |
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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.