FIN Cup System Instrument
Class D (high risk) · MDIR-0007848 · Currax Traders
DRAP REGISTERED MEDICAL DEVICE
FIN Cup System Instrument (Acetabular Components Instrument) is registered with DRAP under number MDIR-0007848 as a Class D (high risk) medical device, imported. The listed holder is Currax Traders. It is listed as valid until 12 Feb 2030.
Screening result
MDIR-0007848 · the class is taken from DRAP's list for this number
DRAP registered Class B/C/D list, 28 Aug 2025
ELI-00716
| Device | FIN Cup System Instrument (Acetabular Components Instrument) |
|---|---|
| Class | D |
| Listed holder | Currax Traders |
| Holder address | House NO. 182, St. No. 02, Scheme No. 7, U-Block, CDL Workshop Railway Pakistan, Rawalpindi |
| Manufacturing site | M/s Gruppo Bioimpianti Srl Via Liguria 28, 20068 Peschiera Borromeo (MI), Italy |
| Issued | 13 Feb 2025 |
| Renewal date | 12 Feb 2030 |
| Licence | ELI-00716 |
Specifications
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Screened 7 Oct 2026, 04:54 (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-0007835 | Janus Cup Acetabular Component | Class D |
| MDIR-0007836 | KORUS Stem Cemented (Femoral Stem hip Component) | Class D |
| MDIR-0007837 | K-MOD PS Fixed Insert Knee component | Class D |
| MDIR-0007838 | K-MOD Patella (Patellar Component Cemented) | Class D |
| MDIR-0007839 | FIN CUP SYSTEM [MB] | Class D |
| MDIR-0007840 | DUALIS System [Acetabular Component Double Mobility Cup] | Class D |
| MDIR-0007841 | K-MOD Knee Instrument (Knee Replacement Instrument) | Class D |
| MDIR-0007842 | K-MOD Fixed Cemented Tibia (PS Cemented Tibial Component) | Class D |
| MDIR-0007843 | K-MOD PS Cemented Femur (PS Fixed Cemented Femoral Component) | Class D |
| MDIR-0007844 | KORUS STEM INSTRUMENT (Femoral Component Instrument) | Class D |
| MDIR-0007845 | MULLER CUP (Acetabular Cemented Cup) | Class D |
| MDIR-0007846 | Femoral CoCr Head for KORUS Stem | Class D |
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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.