Heavy Liquid Infusion Cannulae M4499A

GUDID 25056030401446

25g Perfluorocarbon

STERIMEDIX LIMITED

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

• Primary Device ID: 25056030401446
• NIH Device Record Key: d5de5e88-eef6-4307-bd4b-94c154353822
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Heavy Liquid Infusion Cannulae
• Version Model Number: M4499A-02/10
• Catalog Number: M4499A
• 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	15056030401449 [Primary]
GS1	25056030401446 [Unit of Use]

FDA Product Code

• MED: Sterilant, Medical Devices

Sterilization

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

[25056030401446]

Ethylene Oxide

[25056030401446]

Ethylene Oxide

[25056030401446]

Ethylene Oxide

[25056030401446]

Ethylene Oxide

[25056030401446]

Ethylene Oxide

[25056030401446]

Ethylene Oxide

[25056030401446]

Ethylene Oxide

[25056030401446]

Ethylene Oxide

[25056030401446]

Ethylene Oxide

[25056030401446]

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