EYETEC

Basic Information

• Brand Name: EYETEC
• Primary DI: 00385640052313
• Version / Model: ST40-453-USA
• Company Name: Summit Medical, Inc.
• Labeler DUNS: 965484699
• Distribution Status: In Commercial Distribution
• Device Count in Pkg: 1
• Record Status: Published
• Publish Date: 2022-12-19
• Public Version: 1
• Public Version Date: 2022-12-27
• Public Version Status: New
• Public Device Record Key: 1b068f10-1ee1-49a7-8c59-291112f7fe12

Device Characteristics

• Single Use: Yes
• Prescription Use (Rx): Yes
• Over the Counter (OTC): No
• Kit: No
• Combination Product: No
• HCT/P: No
• Contains NRL: No
• Not Made with NRL: Yes
• MRI Safety: Labeling does not contain MRI Safety Information
• Direct Marking Exempt: No
• PM Exempt: Yes
• Has Serial Number: No
• Has Lot/Batch Number: Yes
• Has Manufacturing Date: No
• Has Expiration Date: Yes
• Has Donation ID: No

Sterilization

• Is Sterile: No
• Sterilization Prior Use: Yes
• Sterilization Methods: Radiation Sterilization

Product Codes

Code	Name	Medical Specialty	Regulation #	Device Class
HOZ	Sponge, Ophthalmic	Ophthalmic	886.4790	2

GMDN Terms

Code	Name	Definition	Implantable	Status
37940	Retina illumination shield	A device typically made of a non-abrasive fluid-absorbing material (e.g., a sponge), intended to be placed on the surface of the cornea to shield the retina from excessive illumination during an ophthalmic procedure; it is not intended to protect the eye from exposure to harmful radiation. It is composed of material that resists the tearing or shredding of its fibres. This is a single-use device.	No	Active

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Package	10385640052310	GS1	Box	200	In Commercial Distribution
Primary	00385640052313	GS1