EVA Nexus Phaco Emulsification NCBF System - DRAP MDIR-0004646 (Class C)

DRAP REGISTERED MEDICAL DEVICE

EVA Nexus Phaco Emulsification NCBF System is registered with DRAP under number MDIR-0004646 as a Class C (moderate to high risk) medical device, imported. The listed holder is AA Enterprises. It is listed as valid until 12 Feb 2028.

Screening result

i
Imported device, registered with DRAP as Class C (moderate to high risk)
MDIR-0004646 · the class is taken from DRAP's list for this number
✓
Found in DRAP's published list
DRAP registered Class B/C/D list, 28 Aug 2025
✓
Listed valid until 12 Feb 2028
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.
DeviceEVA Nexus Phaco Emulsification NCBF System
ClassC
Listed holderAA Enterprises
Holder addressShop No. 57, 15-16 First Floor Mobi Plaza Saddar, Rawalpindi
Manufacturing siteM/s D.O.R.C. Dutch Opthalmic Research Center (International) B.V. Kerkweg 47e, 3214 VC Zuidland, Netherlands. M/s Scheijdelveweg 2 3214 VN Zuidland, the Netherlands
Issued13 Feb 2023
Renewal date12 Feb 2028

Specifications

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Screened 5 Oct 2026, 20:10 (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-0004647EVA Nexus Phaco Vitrectomy NCBF SystemClass C
MDIR-0004648EVA Nexus Phaco Vitrectomy NCBF System With DORC ConnectorClass C
MDIR-0004649EVA Nexus Phaco Vitrectomy NCBF System With SMA ConnectorClass C
MDIR-0004650EVA Combined machine with NCBF SystemClass C
MDIR-0004651EVA Combined machine with NCBF including Laser with SMA connector.Class C
MDIR-0004652Schwind Amaris with models Schwind Amaris 500E Schwind Amaris 750S Schwind Amaris 1050RSClass C
MDIR-0004653FEMTO LDV Z8, FEMTO LDV Z6, FEMTO LDV Z4, FEMTO LDV Z2Class C
MDIR-0005270FEMTO LDV Z6Class C
MDIR-0005271FEMTO LDV Z4Class C
MDIR-0005272FEMTO LDV Z8Class C
MDIR-0006351SCHWING ATOS (Femtosecond Laser for LASIK Surgery) with patient interfaceClass C

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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.