Home Links

The black reusable Bellows (#150), the reusable Headband
(#210, #200), the Tubing (#300), Gauge bulb air pump
(#500, 550) are made of latex.

The Disposable Bellows & Headbands (part series #700’s),
contain:  The Bellows (the blue inflatable cushion) is
100% Polyvinyl Chloride (PVC), which contains no trace of latex.
The Silicone Tubing (#625) is FDA CFR21 177.2600 compliant.  
The white Tyvek® Headband (from DuPont) is polyethylene.
Blue Bulb (#555) is 100% Polyvinyl Chloride  (PVC), does not
contain latex. The Luer Adapter (#650) is acrylic (reusable).
Caution: This Product Contains
Natural Rubber Latex  Which May
Cause Allergic Reactions
Added Safety in Phaco Emulsification

The instrument can be used before and/or after retrobulbar, peribulbar or subtenons anesthesia.  Application after injection
anesthesia, or pledgets soaked in topical anesthetic solution and positions in cul-de-sacs, can enhance the effect of the
anesthesia.  Softening the eye, by presurgery ocular compression prior to phaco emulsification in small incision, no-suture surgery,
can be a safety feature in occasional cases where conversion to extracapsular or intracapsular surgery is necessary.

Preoperative ocular compression may be a safety measure in preventing choroidal expulsive hemorrhage.  Sudden stress
occurs on fragile sclerotic vessels when the intraocular pressure is suddenly reduced to atmospheric pressure at the time of
incision. Lowering the intraocular pressure by preoperative ocular compression should reduce the pressure differential and the
amount of stress on the vessels at time of incision.
EU Authorized Representative:
D.R.M. Green
Eurolink (Europe) Ltd.
Greyfriars Court
Paridise Square
Oxford, Oxon OX1 1BE
United Kingdom

Tel:(44) 179 378 4545
Fax: (44) 179 378 4551
Above logo is a link to
Eurolink (Europe) Ltd.
The device is classified as a Class I
unsterilised medical device and a notified
EU body is not involved in its certification.  
Therefore there is no certificate from a
notified body.  
Customer Service Hours
8 am - 5 pm  EDST Monday - Thursday
8 am - 4 pm  EDST Friday
(New York time)

(USA & Canada)


(printer friendly)

Pressure on the eye traditionally has been a method of slowing some tachycardias.  Some persons may be more sensitive to the
ocular-vagal reflex.  Therefore, all patients should be monitored for signs of bradycardia while pressure is being applied to the eye.

The optimum pressure to be used should be well below pressure in the central retinal artery.  It should be elevated only high
enough to create a soft surgical eye.  Using the 20 to 30 mm Hg of monitored pressure for 30 to 60 minutes before surgery,
clinically results in very soft, safe, surgical eyes.  With the Schiotz Tonometer with 5.5 gram weight, the scale reading may be
above 10.  An eye may be so soft that the cornea may be observed to dimple when the lid speculum is inserted. Releasing the
pressure every 30 seconds and then reapplying it has NOT been found necessary or desirable.

With a soft eye, the iris may be concave or drop posteriorly after lens removal.  Excess vitreous pressure is typically absent.  
Intraocular lens implantation is much easier and safer.  From the surgeon’s viewpoint, there is much less stress and strain.
Preparation for use

Clean and disinfect the Headband, Bellows and Tubing (parts that
touch the patient’s face) using CaviCide® (from Metrex), Matar®
(from ECOLAB, INC.) or a recognized germicidal solution.
Wipe clean. Do not immerse. Do not autoclave or gas sterilize.
Flag Counter