Vitreoretinal Cannulae M4477

GUDID 15056030401302

25g x 1 1/4" Asp Cann

STERIMEDIX LIMITED

Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use

• Primary Device ID: 15056030401302
• NIH Device Record Key: 091ed988-8e64-44e0-91c4-bed6cc5bcf93
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Vitreoretinal Cannulae
• Version Model Number: M4477-02/10
• Catalog Number: M4477
• Company DUNS: 504799313
• Company Name: STERIMEDIX LIMITED
• Device Count: 10
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	15056030401302 [Unit of Use]
GS1	25056030401309 [Primary]

FDA Product Code

• MED: Sterilant, Medical Devices

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: true

[15056030401302]

Ethylene Oxide

[15056030401302]

Ethylene Oxide

[15056030401302]

Ethylene Oxide

[15056030401302]

Ethylene Oxide

[15056030401302]

Ethylene Oxide

[15056030401302]

Ethylene Oxide

[15056030401302]

Ethylene Oxide

[15056030401302]

Ethylene Oxide

[15056030401302]

Ethylene Oxide

[15056030401302]

Ethylene Oxide

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-10-15
• Device Publish Date: 2024-10-07

On-Brand Devices [Vitreoretinal Cannulae]

• 35056030401009: 23g x 1 1/4" Asp Cann
• 35056030400996: 23g x 4mm VFI
• 25056030401019: 25g Silicone Brush
• 15056030401302: 25g x 1 1/4" Asp Cann