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PMMA AC (Anterior Chamber)
PMMA AC (Anterior Chamber)
PMMA AC (Anterior Chamber)
PMMA AC (Anterior Chamber)
PMMA AC (Anterior Chamber)
PMMA AC (Anterior Chamber)

PMMA AC (Anterior Chamber)

MOQ : 1 Unit

PMMA AC (Anterior Chamber) Specification

  • Equipment Type
  • Anterior Chamber Intraocular Lens (IOL)
  • Material
  • PMMA (Polymethyl Methacrylate)
  • Technology
  • Single-Piece Rigid Lens
  • Properties
  • High optical clarity, UV absorbent
  • Grade
  • Medical grade PMMA
  • Lens Specification
  • Angled haptics, one-piece design
  • Lens Diameter
  • 6.0 mm
  • Implants Specifications
  • For use in anterior chamber implantation
  • Driven Method
  • Manual insertion
  • Dimension (L*W*H)
  • Overall length approx. 12.5 mm
  • Weight
  • Lightweight (precise value not specified)
  • Usage
  • Used in cataract surgery to replace natural lens in anterior chamber
  • Sterilized
  • Yes
  • Sterilization Mode
  • Ethylene Oxide (ETO) Sterilized
  • Packaging
  • Sterile, single-use blister pack
  • Optic Design
  • Monofocal, non-foldable
  • Model
  • PMMA-AC
  • Shelf Life
  • 3-5 years
  • Refractive Index
  • 1.49
  • Diopter Range
  • +10 D to +30 D (varies by model)
  • Color
  • Clear (Colorless)
  • Haptic Type
  • Angled PMMA haptics
 

PMMA AC (Anterior Chamber) Trade Information

  • Minimum Order Quantity
  • 1 Unit
  • Supply Ability
  • 5000 Units Per Day
  • Delivery Time
  • 7-20 Days
 

About PMMA AC (Anterior Chamber)

Details of the product ;-



MODEL

 PAC

Optic Diameter

6.00 mm

Overall Diameter

12.50 mm

Optic Design

Spherical Biconvex

Hoptic Design

SDesign With Step Vault

Dialing Holes

Nil

Suggested A. Constant

115.3





High Optical Clarity and Durability

Manufactured from medical-grade PMMA, the PMMA AC IOL stands out for its excellent optical clarity and robust durability. The rigid, single-piece construction and angled haptics enable reliable fixation and long-term stability within the anterior chamber. Patients and surgeons benefit from a clear, colorless lens that ensures optimal vision correction and dependable performance.


Sterile Packaging and Simple Insertion

Every PMMA AC lens is supplied in a sterile, single-use blister pack, minimizing the risk of contamination during surgery. The lens is designed for manual insertion, a standard and straightforward procedure for ophthalmic professionals. Its high biocompatibility and ethylene oxide sterilization further ensure patient safety and surgical convenience.

FAQs of PMMA AC (Anterior Chamber):


Q: How is the PMMA AC (Anterior Chamber) IOL implanted during cataract surgery?

A: The PMMA AC IOL is manually inserted into the anterior chamber of the eye after removal of the natural lens, typically during cataract surgery. Its angled PMMA haptics provide secure placement and help maintain stability within the anterior chamber.

Q: What are the main benefits of using a PMMA AC IOL with angled haptics?

A: Angled haptics in the PMMA AC IOL ensure improved stability and proper positioning within the anterior chamber. The lens also offers high optical clarity, UV protection, and long-term durability, benefiting both the patient and the surgeon.

Q: When should an anterior chamber intraocular lens be considered?

A: Anterior chamber IOLs like the PMMA AC are often considered when a posterior chamber IOL cannot be placed, such as in cases with insufficient capsular support or complications during cataract surgery.

Q: Where is the PMMA AC IOL manufactured and supplied?

A: The PMMA AC IOL is manufactured, exported, supplied, and traded in India, enabling reliable distribution and access for ophthalmic clinics and surgical centers throughout the region.

Q: What is the shelf life and packaging method of PMMA AC IOLs?

A: These lenses are packaged in sterile, single-use blister packs and have a shelf life of three to five years, ensuring safe storage and use in surgical settings.

Q: What is the process of ensuring sterility for the PMMA AC IOL?

A: The PMMA AC IOL undergoes ethylene oxide (ETO) sterilization, a widely recognized method in medical device preparation, ensuring that each lens remains free from microbial contamination before implantation.

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