ISO13485 HEMA PMMA Foldable Intraocular Lens For Cataract Surgery
Price
negotiation
MOQ
1000 pcs
Delivery Time
7 working days
Brand
Universe IOL
Place of Origin
China
Certification
ISO13485,ISO9001
Model Number
PCF60
Packaging Details
170 pcs per box(Size:47x48x39cm)
Payment Terms
T/T
Supply Ability
10000 pcs per month
Product Details
Product Specification
Place of Origin
China
Packaging Details
170 pcs per box(Size:47x48x39cm)
Water Contents
26%
Body diameter
6.0mm
Material
Hydrophilic Acrylic
Model Number
PCF60
Supply Ability
10000 pcs per month
Certification
ISO13485,ISO9001
Overall diameter
12.5mm
Brand Name
Universe IOL
Payment Terms
T/T
Price
negotiation
Delivery Time
7 working days
Minimum Order Quantity
1000 pcs
Model
PCF60
Power
0-30D
Product Description
Hydrophilic Acrylic Foldable Intraocular Lens with Water Contents 26%
Hydrophilic Acrylic Foldable Intraocular Lens with Water Contents are copolymers of HEMA and PMMA, with water contents of 26%, and are much more resistant to deformation and opacification.
Material:
Hydrophilic Acrylic
Water Contents:
26%
Model:
PCF60
Body Diameter:
6.0mm
Overall Diameter:
12.5mm
Power:
0-30D
Indications:
Cataract on both eyes.
Cataract of single eye in patients, who is unwilling or unfitful to wear corneal contact lens
Aphakic eye caused by various reasons
Instruction for Use
Examine the type, diopter power, size, the period of validity indicated on the outside package label. DO NOT USE if the expiration date has passed.
Take out the tyvek pounch and check that there is no damage on it, verify that lens power, size, type on the vial are same with the data on the outside label.
Open the pounch under the aseptic place, open the lens case after final confirmation of lens model and diopter power, take out IOL very carefully and implant IOL into eyes.
Rinse the IOL with infusion solution or the equivalent.
Precautions
Do not use the One-piece Posterior Chamber Foldable Intraocular Lens if it is after expiration date.
Do not try to re-sterilize the One-piece Posterior Chamber Foldable Intraocular Lens.
The surgeon must be the person who had observed and assisted IOL implantation surgery many times, must be also the person , who has been ophthalmologist with rich experience and independently completed the IOL omplantation successfully for at least one time.
