Stryker Craniomaxillofacial | MEDPOR Biomaterial Ophthalmic Series | Porous High-Density Polyethylene | Model 9778 | Small Size Variant (19 mm x 22 mm x 4.4 mm Dimensions) | Vented Ocular Conformer

Expiration Date 11-30-2027

The Stryker Medpor 9778 is a professional-grade, sterile, biocompatible oculoplastic conformer manufactured from an advanced porous high-density polyethylene biomaterial and precision-engineered as a small-size 19 mm x 22 mm x 4.4 mm anatomical vault shield designed to preserve the physical structure of the conjunctival cul-de-sacs and mucosal fornices following extensive enucleation, evisceration, or orbital socket reconstructions. Intended for short-term clinical placement during the primary post-operative healing window, this non-reactive polymer template maintains the structural volume of the socket and actively prevents tissue contraction, scarring adhesion bands, or symblepharon formation without putting mechanical pressure on the eyelid margin. The specialized vented layout features built-in drainage holes that facilitate the seamless instillation of topical antibiotic drops or ointments while promoting the free escape of surgical fluids and dynamic secretions, eliminating the necessity of removing the shield during routine wound assessments and providing an optimal, integrated soft-tissue foundation for the subsequent alignment of a permanent cosmetic ocular prosthesis.

Technical Specifications

• Manufacturer: Stryker Craniomaxillofacial (Stryker Corporation CMF/Trauma Division)

• Product Brand Family: MEDPOR Oculoplastic Biomaterial Series / Vented Conformer Portfolio

• Product Catalog Code (MPN): 9778 (Often indexed under stock string SKU SYK9778 or SYK9778-SD)

• Device Material Composition: Porous High-Density Polyethylene (HDPE Biomaterial)

• Structural Sizing Allocation: Small Size Variant

• Physical Dimensions: 19 mm width x 22 mm height x 4.4 mm thickness nominal

• Conformer Geometry Layout: Anatomically curved convex/concave rigid shield incorporating multiple circular drainage vents

• Sterility Presentation Status: Arrives individually packaged, factory-sealed, and pre-sterilized via validated cycles for rapid single-use operating room deployment

• Operational Reuse Classification: Strictly Single-Use Disposable (Discard following initial clinical extraction cycle)

• Re-Sterilization Restriction: Strictly non-autoclavable; must never be exposed to secondary thermal autoclave loops