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eyeWatch implant

eyeWatch

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For IFU in other languages, contact Rheon Medical.

The eyeWatch system is indicated for patients suffering from glaucoma where medical and/or conventional surgical treatments have failed. The eyeWatch system is intended to drain aqueous humor from the anterior chamber to the subconjunctival space and to regulate non-surgically the intraocular pressure during the early post-operative period.

The implantation of the eyeWatch implant is contraindicated if one or more of the following conditions exist:

  • Diagnosis of angle-closure glaucoma, neovascular glaucoma.
  • Patient with ocular malformations such as microphthalmia.
  • Patient with corneal opacifications or irregularities that may interfere with IOP measurements.
  • History of previous corneal transplant surgery.
  • Patient with concurrent inflammatory/infective eye disorder.

The eyewatch is MR Conditional

MR Conditions:

  • Horizontal bore MR system with a static magnetic field of 1.5 Tesla or 3 Tesla.
  •  Gradient magnetic fields lower or equal to 19 T/m.
  • Whole body averaged SAR (Specific Absorption Rate) limited to Normal Operating Mode (WB-SAR ≤2W/kg).
  • The association eyeWatch + eyePlate is expected to produce a maximum temperature rise of 2°C at both 1.5T and 3T for a WB-SAR of 2W/kg after 1h of continuous scanning

eyePlate

eyePlate

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For IFU in other languages, contact Rheon Medical.

The eyePlate is intended to manage intraocular pressure in glaucoma patients where medically controlled glaucoma or filtering surgery have failed or are likely to fail, such as, but not limited to, neovascular glaucoma, aphakic/pseudophakic glaucoma, uveitic glaucoma, congenital glaucoma, etc.

Conjunctivitis, corneal ulcers, endophthalmitis, orbital cellulitis, bacteremia or septicemia, active scleritis, active uveitis, scleral buckle, rectus muscle surgery.

   The eyePlate is MR safe

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