DRAP REGISTERED MEDICAL DEVICE
CERABLATE Easy/TC Cardiac Ablation Catheter is registered with DRAP under number MDIR-0000405 as a Class D (high risk) medical device, imported. The listed holder is Alliance Medical. Its listed renewal date (28 May 2024) has passed, so ask the supplier for the renewal letter.
Screening result
MDIR-0000405 · 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-00147
| Device | CERABLATE Easy/TC Cardiac Ablation Catheter |
|---|---|
| Class | D |
| Listed holder | Alliance Medical |
| Holder address | 12-B, 1st Floor, Agro Flats, Shadman, Lahore |
| Manufacturing site | M/s. OSYPKA AG Earl-H, Wood-Strasse 1, 79618 Rheinfelden, Germany |
| Issued | 29 May 2019 |
| Renewal date | 28 May 2024 |
| Licence | ELI-00147 |
Specifications
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Screened 5 Oct 2026, 22:15 (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-0000243 | ARIES Three Stop Extension Line (Pressure Extension Line) (Extension Line) | Class A |
| MDIE-0000244 | GENOSS Inflator Set (Catheter Balloon) | Class A |
| MDIR-0000223 | Embolectomy Catheter | Class B |
| MDIR-0000224 | Accutarans Pressure Monitoring Systems and Kits | Class B |
| MDIR-0000225 | Central Venous Catheter and Catheterization Kit | Class B |
| MDIR-0000396 | Biosensors Thermodilution Catheter and kit | Class D |
| MDIR-0000397 | Biosensors Bipolar Pacing Catheter | Class D |
| MDIR-0000400 | SELDICATH Arterial Catheter | Class D |
| MDIR-0000401 | OSYPKA TME Temporary Myocardial Electrode (Heart Wire) | Class D |
| MDIR-0000402 | CERABLATE Cool Cardiac Ablation Catheter | Class D |
| MDIR-0000403 | FINDER/Pure Intracardiac Diagnostic Catheter | Class D |
| MDIR-0000404 | VACS Percutaneous Transluminal Valvuloplasty Balloon 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.
