DRAP REGISTERED MEDICAL DEVICE
Eyekon (PMMA Posterior Chamber Intraocular Lens) [S-116, S-104] is registered with DRAP under number MDIR-0007026 as a Class C (moderate to high risk) medical device, imported. The listed holder is Medi-Serv International. It is listed as valid until 8 Aug 2029.
Screening result
MDIR-0007026 · the class is taken from DRAP's list for this number
DRAP registered Class B/C/D list, 28 Aug 2025
ELI-00171
| Device | Eyekon (PMMA Posterior Chamber Intraocular Lens) [S-116, S-104] |
|---|---|
| Class | C |
| Listed holder | Medi-Serv International |
| Holder address | GF 28 Jinnah Plaza, Defence Chowk, Main Boulevard Lahore Cantt |
| Manufacturing site | M/s Eyekon Medical Inc., 2451 Enterprise Road, Clearwater, FL USA 33763 |
| Issued | 9 Aug 2024 |
| Renewal date | 8 Aug 2029 |
| Licence | ELI-00171 |
Specifications
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Screened 6 Oct 2026, 06:04 (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-0007024 | Eyekon (Posterior Chamber Intraocular Lenses (Hydrophilic Acrylic) | Class C |
| MDIR-0007025 | Eyekon Viscoelastic Gel (Ophthalmic viscosurgical device) [Eyecoat] | Class B |
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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.