ULTRA FLOW

GUDID 00380657517954

ULTRAFLOW II I/A HANDPIECE

Alcon Laboratories, Inc.

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

• Primary Device ID: 00380657517954
• NIH Device Record Key: 7b3321ed-ec03-4b3b-b59a-ab0c2ef5574d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ULTRA FLOW
• Version Model Number: 8065751795
• Company DUNS: 008018525
• Company Name: Alcon Laboratories, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)862-5266
• Email: web.masterus@alcon.com
• Phone: +1(800)862-5266
• Email: web.masterus@alcon.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00380657517954 [Primary]

FDA Product Code

• NKK: NEEDLE, HYPODERMIC, SINGLE LUMEN, REPROCESSED

Sterilization

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

[00380657517954]

Moist Heat or Steam Sterilization

[00380657517954]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 6
• Public Version Date: 2019-10-07
• Device Publish Date: 2017-06-07

On-Brand Devices [ULTRA FLOW]

• 00380658176013: ULTRAFLOW S/P CURVED TIP, .3 mm
• 00380658173012: ULTRAFLOW S/P 90 BENT TIP, .3 mm
• 00380658172015: ULTRAFLOW S/P 45 BENT TIP, .3MM
• 00380658170011: ULTRAFLOW S/P STRAIGHT TIP, .3MM
• 00380657517954: ULTRAFLOW II I/A HANDPIECE