DRAP REGISTERED MEDICAL DEVICE
Lumixa (Ophthalmic solution) is registered with DRAP under number MDIR-0000870 as a Class C (moderate to high risk) medical device, imported. The listed holder is Hakimsons (Pvt) Ltd.. Its listed renewal date (10 Sep 2024) has passed, so ask the supplier for the renewal letter.
Screening result
MDIR-0000870
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-00396
| Device | Lumixa (Ophthalmic solution) |
|---|---|
| Class | C |
| Listed holder | Hakimsons (Pvt) Ltd. |
| Holder address | A-58/B, SITE, Mangophir Road, Karachi |
| Manufacturing site | M/s Omisan Farmaceutici Via Galileo Galilei snc, 00012 Guidonia Montecelio (RM), Italy |
| Issued | 10 Oct 2019 |
| Renewal date | 10 Sep 2024 |
| Licence | ELI-00396 |
Specifications
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Screened 5 Oct 2026, 09:28 (Pakistan time). A screening aid, not an official DRAP verification.
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Other DRAP registrations and enlistments listed for the same company.
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| MDIR-0004951 | Foyomed Burette Infusion set | Class B |
| MDIR-0004952 | Foyomed Stomach tube | Class B |
| MDIR-0004953 | Foyomed Reinforced Endotracheal tube, cuffed | Class B |
Similar devices from other companies
Same device type listed by other holders, useful when comparing suppliers.
| MDIR-0004347 | LUMIXA Advanced (Cross linked Hyaluronic acid 0.15% Crocin & Liposomes) | Class C | De Khon |
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.
