DRAP REGISTERED MEDICAL DEVICE
GRAFTMASTER RX Coronary Stent Graft System is registered with DRAP under number MDIR-0003421 as a Class D (high risk) medical device, imported. The listed holder is Digital Imaging Systems. It is listed as valid until 8 Jun 2027.
Screening result
i
Number type: imported, registered (Class B, C or D)
MDIR-0003421
MDIR-0003421
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Found in DRAP's published list
DRAP registered Class B/C/D list, 28 Aug 2025
DRAP registered Class B/C/D list, 28 Aug 2025
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Listed valid until 8 Jun 2027
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Holder has a DRAP import licence on file
ELI-00094
ELI-00094
| Device | GRAFTMASTER RX Coronary Stent Graft System |
|---|---|
| Class | D |
| Listed holder | Digital Imaging Systems |
| Holder address | 121- Habitat Apartments, Shadman II, Ghaus-ul-Azam Road, Lahore |
| Manufacturing site | M/s Abbott Vascular 3200 Lakeside Drive Santa Clara, CA 95054, USA M/s Abbott Vascular Cashel Road, Clonmel, Co. Tipperary, Ireland |
| Issued | 9 Jun 2022 |
| Renewal date | 8 Jun 2027 |
| Licence | ELI-00094 |
Specifications
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Screened 4 Oct 2026, 23:52 (Pakistan time). A screening aid, not an official DRAP verification.
More devices from this holder
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| MDIR-0000010 | NC Trek RX Coronary Dilatation Catheter | Class D |
| MDIR-0000011 | Mini Trek RX Coronary Dilatation Catheter | Class D |
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| MDIR-0000013 | RX Herculink Elite Peripheral Stent System | Class C |
| MDIR-0000014 | RX Acculink Carotid Stent System | Class D |
| MDIR-0000015 | Omnilink Elite Peripheral Stent System | Class C |
| MDIR-0000016 | Hi-Torque Whisper Guide Wire with Hydrophilic Coating | Class D |
| MDIR-0000017 | Hi-Torque Balance Middle Weight Guide Wire | 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.