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Company Name Brand Name GMDN Term Name GMDN Term Status FDA Product Code Name FDA Product Code Device Packaged As Sterile Sterilization Prior To Use Issuing Agency Device Size Device Size Type Device Class Implantable

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MONARCH® III - 00380659777738

MONARCH III IOL DELIVERY SYSTEM, INJECTOR
Alcon Laboratories, Inc.
8065977773
In Commercial Distribution

  • 00380659777738 ()


  • Manual intraocular lens injector, reusable

MONARCH® III - 00380659777639

The Monarch® "D" Cartridge is a single-use polypropylene cartridge for posterior chamber IOL delivery
Alcon Laboratories, Inc.
8065977763
In Commercial Distribution

  • 10380659777636 ()
  • 00380659777639 ()


  • Intraocular lens-insertion cartridge

MONARCH® - 00380659777622

The Monarch® III "C" Cartridge is a single-use polypropylene cartridge for posterior chamber IOL delivery.
Alcon Laboratories, Inc.
8065977762
In Commercial Distribution

  • 10380659777629 ()
  • 00380659777622 ()


  • Intraocular lens-insertion cartridge

MONARCH® II - 00380659777578

The Monarch® "A" Cartridge is a single-use polypropylene cartridge for posterior chamber IOL delivery
Alcon Laboratories, Inc.
8065977757
In Commercial Distribution

  • 10380659777575 ()
  • 00380659777578 ()


  • Intraocular lens-insertion cartridge

ClearCut® - 00380659215407

ClearCut® Sideport Knife Dual Bevel 1.0mm Angled
Alcon Laboratories, Inc.
8065921540
In Commercial Distribution

  • 10380659215404 ()
  • 00380659215407 ()


  • Ophthalmic knife, single-use

I-Knife - 00380659215179

I-Knife Cutting Instrument Mackool Sideport Knife
Alcon Laboratories, Inc.
8065921517
Not in Commercial Distribution

  • 10380659215176 ()
  • 00380659215179 ()


  • Ophthalmic knife, single-use

V-Lance - 00380659119019

Ophthalmic Corneal/Scleral V-Lance Knife 19 Gauge [1.6mm]
Alcon Laboratories, Inc.
8065911901
In Commercial Distribution

  • 10380659119016 ()
  • 00380659119019 ()


  • Ophthalmic knife, single-use

WaveLight - 00380659984372

Diagnostic device to perform non-contact measurements of the corneal tomography, anterior chamber parameter, pupil diameter, axial length, and optical aberrations of the patient’s eye.
Alcon Laboratories, Inc.
1023
In Commercial Distribution

  • 00380659984372 ()
8065998437

  • Eye anterior segment analyser

ORA System® VerifEye™ - 00380659983283

ORA System with VerifEyeTM+, Aberometer 190.5
Alcon Laboratories, Inc.
8065998328
In Commercial Distribution

  • 00380659983283 ()


  • Automated ophthalmic refractometer

WaveLight - 00380659982989

WAVELIGHT FS200 PATIENT INTERFACE - EASYPACK (BOX OF 20)
Alcon Laboratories, Inc.
8065998298
In Commercial Distribution

  • 00380659982989 ()
  • 00380659982996 ()


  • Ophthalmic surgical procedure kit, non-medicated, single-use
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