Heavy Liquid Infusion Cannulae M4453

GUDID 15056030401050

25g x 7mm VFI Cannula

STERIMEDIX LIMITED

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

• Primary Device ID: 15056030401050
• NIH Device Record Key: 18a7e61c-8d2a-4c92-b3f2-350f6ffa02de
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Heavy Liquid Infusion Cannulae
• Version Model Number: M4453-02/10
• Catalog Number: M4453
• 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	15056030401050 [Unit of Use]
GS1	25056030401057 [Primary]

FDA Product Code

• MED: Sterilant, Medical Devices

Sterilization

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

[15056030401050]

Ethylene Oxide

[15056030401050]

Ethylene Oxide

[15056030401050]

Ethylene Oxide

[15056030401050]

Ethylene Oxide

[15056030401050]

Ethylene Oxide

[15056030401050]

Ethylene Oxide

[15056030401050]

Ethylene Oxide

[15056030401050]

Ethylene Oxide

[15056030401050]

Ethylene Oxide

[15056030401050]

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 [Heavy Liquid Infusion Cannulae ]

• 15056030401050: 25g x 7mm VFI Cannula
• 15056030401043: Viscous Fluid Injection
• 25056030401446: 25g Perfluorocarbon
• 25056030401439: 23g Perfluorocarbon Cann