DRAP REGISTERED MEDICAL DEVICE
Therapy Ablation Catheters is registered with DRAP under number MDIR-0000731 as a Class D (high risk) medical device, imported. The listed holder is Physiomed (Pvt) Ltd.. Its listed renewal date (28 Jun 2026) has passed, so ask the supplier for the renewal letter.
Screening result
MDIR-0000731
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-00199
| Device | Therapy Ablation Catheters |
|---|---|
| Class | D |
| Listed holder | Physiomed (Pvt) Ltd. |
| Holder address | 268/3, Kamal Road, Saddar,Rawalpindi., Godown Address: Same as above |
| Manufacturing site | M/s. Irvine Biomedical Inc St. Jude Medical Company, 2375, Morse Avenue, Irvine CA, 92614, USA |
| Issued | 29 Jun 2021 |
| Renewal date | 28 Jun 2026 |
| Licence | ELI-00199 |
Specifications
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Screened 5 Oct 2026, 12:10 (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-0000200 | Endurity Core CRT-Ps Implantabale Cardiac Pulse Generators (Pacemakers) [PM1152, PM2152] | Class D |
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| MDIR-0000202 | Fortify AssuraTM DR [CD2359-40Q, CD2359-40QC, MR Conditional] | Class D |
| MDIR-0000203 | Ellipse TM VR [CD1377-36Q, CD1377-36QC] | Class D |
| MDIR-0000204 | Quadra Allure MP RF CRT-P) [PM 3262] | Class D |
| MDIR-0000205 | Tendril STS Implantable Cardiac Pacing Leads (Bradycardia and Left Heart Leads) [2088TC] | Class D |
| MDIR-0000206 | Quadra Assura TM [CD3367-40, CD3367-40C] | Class D |
| MDIR-0000207 | Durata TM [7121Q-58, 7120Q-65] | Class D |
| MDIR-0000208 | Quartet TM [1456Q-75] | Class D |
| MDIR-0000726 | CPS AimTM SL (Sittable Inner Catheter) with integrated valve | Class D |
| MDIR-0000727 | Advisor FL Circular Mapping Catheter, Sensor Enabled (Circular Mapping Catheter) | Class D |
| MDIR-0000728 | Livewire Streerable Electrophysiology Catheter | Class D |
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.