23G High Flow infusion line 1279.HF23-00

GUDID 18717872034932

D.O.R.C. Dutch Ophthalmic Research Center (International) B.V.

Ophthalmic cannulation set, single-use Ophthalmic cannulation set, single-use Ophthalmic cannulation set, single-use Ophthalmic cannulation set, single-use Ophthalmic cannulation set, single-use Ophthalmic cannulation set, single-use Ophthalmic cannulation set, single-use Ophthalmic cannulation set, single-use Ophthalmic cannulation set, single-use Ophthalmic cannulation set, single-use Ophthalmic cannulation set, single-use Ophthalmic cannulation set, single-use Ophthalmic cannulation set, single-use Ophthalmic cannulation set, single-use Ophthalmic cannulation set, single-use Ophthalmic cannulation set, single-use Ophthalmic cannulation set, single-use Ophthalmic cannulation set, single-use Ophthalmic cannulation set, single-use Ophthalmic cannulation set, single-use Ophthalmic cannulation set, single-use Ophthalmic cannulation set, single-use Ophthalmic cannulation set, single-use Ophthalmic cannulation set, single-use Ophthalmic cannulation set, single-use Ophthalmic cannulation set, single-use Ophthalmic cannulation set, single-use Ophthalmic cannulation set, single-use Ophthalmic cannulation set, single-use Ophthalmic cannulation set, single-use

• Primary Device ID: 18717872034932
• NIH Device Record Key: 7fa59457-bdda-49c2-a3da-4fbb0a981470
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 23G High Flow infusion line
• Version Model Number: 1279.HF23-00
• Catalog Number: 1279.HF23-00
• Company DUNS: 407522184
• Company Name: D.O.R.C. Dutch Ophthalmic Research Center (International) B.V.
• Device Count: 6
• 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	08717872034935 [Primary]
GS1	18717872034932 [Unit of Use]

FDA Product Code

• NGY: Cannula, Trocar, Ophthalmic

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-02-29
• Device Publish Date: 2024-02-21

On-Brand Devices [23G High Flow infusion line]

• 18717872032396: 1279.HF23
• 18717872034932: 1279.HF23-00