AQUA SIY - DRAP MDIR-0003851 (Class C)

DRAP REGISTERED MEDICAL DEVICE

AQUA SIY (Posterior chamber intraocular lens) is registered with DRAP under number MDIR-0003851 as a Class C (moderate to high risk) medical device, imported. The listed holder is Medoptics. It is listed as valid until 24 Oct 2027.

Screening result

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Number type: imported, registered (Class B, C or D)
MDIR-0003851
✓
Found in DRAP's published list
DRAP registered Class B/C/D list, 28 Aug 2025
✓
Listed valid until 24 Oct 2027
i
Holder not found in DRAP's published licence list
That list covers manually issued licences only. Ask for a copy of the establishment licence.
DeviceAQUA SIY (Posterior chamber intraocular lens)
ClassC
Listed holderMedoptics
Holder addressFlat No. 3, 3rd Floor, Hafiz Plaza, M-Block, Model Town, Lahore.
Manufacturing siteM/s Aaren Scientific Inc. 1040 S. Vintage Ave. Bldg.A Ontario, CA 91761 USA
Issued25 Oct 2022
Renewal date24 Oct 2027

Specifications

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Screened 5 Oct 2026, 06:38 (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.

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MDIR-0008461MEDA Ultrasonic A/B Scanner for Ophthalmology ODM-2200Class B
MDIR-0008462PreciSAL Soft Hydrophobic Acrylic Intraocular Lens Preloaded [SAL PS302A]Class C
MDIR-0008463PreciSAL Soft Hydrophobic Acrylic Intraocular Lens [SAL 302A]Class C

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Same device type listed by other holders, useful when comparing suppliers.

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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.