Hydrodissection Cannulae M3992

GUDID 55056030400969

30g x 7/8" Hydrodissector

STERIMEDIX LIMITED

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

• Primary Device ID: 55056030400969
• NIH Device Record Key: 35b80b8d-1d07-425e-8310-1282b8bfdcbd
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Hydrodissection Cannulae
• Version Model Number: M3992-02
• Catalog Number: M3992
• 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	15056030400961 [Primary]
GS1	55056030400969 [Unit of Use]

FDA Product Code

• MED: Sterilant, Medical Devices

Sterilization

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

[55056030400969]

Ethylene Oxide

[55056030400969]

Ethylene Oxide

[55056030400969]

Ethylene Oxide

[55056030400969]

Ethylene Oxide

[55056030400969]

Ethylene Oxide

[55056030400969]

Ethylene Oxide

[55056030400969]

Ethylene Oxide

[55056030400969]

Ethylene Oxide

[55056030400969]

Ethylene Oxide

[55056030400969]

Ethylene Oxide

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-02-25
• Device Publish Date: 2025-02-17

On-Brand Devices [Hydrodissection Cannulae]

• 35056030400781: 25g Tapered Hydro
• 55056030400969: 30g x 7/8" Hydrodissector