EVA NEXUSTM Custom Phaco Pack 1.8mm 45 (Straight)

GUDID 18717872034352

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

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• Primary Device ID: 18717872034352
• NIH Device Record Key: d11a3202-99db-45be-92a0-1b359079a48b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: EVA NEXUSTM Custom Phaco Pack 1.8mm 45 (Straight)
• Version Model Number: 9545.18SF1
• 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: 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: 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	08717872034355 [Primary]
GS1	18717872034352 [Unit of Use]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K213467

FDA Product Code

• HQC: Unit, Phacofragmentation

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: 2022-10-17
• Device Publish Date: 2022-10-07

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

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• 18717872034949 - 25G High Flow infusion line: 2024-02-29
• 18717872034956 - 27G High Flow infusion line: 2024-02-29
• 18717872035106 - EVA NEXUS™ Posterior 23G TDC Pack: 2024-02-29
• 18717872035113 - EVA NEXUS™ Posterior 25G TDC Pack: 2024-02-29
• 18717872035120 - EVA NEXUS™ Posterior 27G TDC Pack: 2024-02-29
• 18717872035304 - EVA NEXUS™ Posterior 23G TDC Pack: 2024-02-29
• 18717872035311 - EVA NEXUS™ Posterior 25G TDC Pack: 2024-02-29