DRAP REGISTERED MEDICAL DEVICE
Cardiohealth Guiding Catheter [GC6AL1, GC6AL2, GC6AR1, GC6AR2, GC6EBU30, GC6EBU35, GC6EBU40, GC6IMA, GC6JL35, GC6JL40, GC6JL45, GC6JR35, GC6JR40, GC6JR45, GC6MPA] is registered with DRAP under number MDIR-0009788 as a Class B (low to moderate risk) medical device, imported. The listed holder is Health Tec. It is listed as valid until 23 Jul 2030.
Screening result
MDIR-0009788 · the class is taken from DRAP's list for this number
DRAP registered Class B/C/D list, 28 Aug 2025
ELI-00046
| Device | Cardiohealth Guiding Catheter [GC6AL1, GC6AL2, GC6AR1, GC6AR2, GC6EBU30, GC6EBU35, GC6EBU40, GC6IMA, GC6JL35, GC6JL40, GC6JL45, GC6JR35, GC6JR40, GC6JR45, GC6MPA] |
|---|---|
| Class | B |
| Listed holder | Health Tec |
| Holder address | House No. 10-B, Street 24, Valley Road, Westridge 1, Rawalpind |
| Manufacturing site | M/s Cardiohealth, Asik Veysel Mahallesi 5821/1 Sokak. No:6, Karabaglar Izmir, Turkey |
| Issued | 24 Jul 2025 |
| Renewal date | 23 Jul 2030 |
| Licence | ELI-00046 |
Specifications
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Screened 6 Oct 2026, 14:51 (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-0000054 | Xlimus Sirolimus Eluting Coronary Stent System | Class D |
| MDIR-0000266 | Pointer Angiographic Catheter | Class D |
| MDIR-0000267 | Accoat Guidewire | Class D |
| MDIR-0000268 | Poseidon Hydrophilic Nitinol Guide Wire | Class D |
| MDIR-0000879 | SCW Hemostasis Valve Sets | Class B |
| MDIR-0000880 | SCW Transradial Introducer Sets | Class B |
| MDIR-0000881 | SCW Introducer Sets | Class B |
| MDIR-0000882 | SCW Guide Wire | Class B |
| MDIR-0002654 | SCW (Balloon Inflation Device) | Class B |
| MDIR-0004615 | EVEREST SC (PTCA Balloon Dilatation Catheter) | Class D |
| MDIR-0004616 | FORCE NC (PTCA Balloon Dilatation Catheter Non-complaint) | Class D |
| MDIR-0004617 | SUMMIT CTO (PTCA Balloon Dilatation 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.
