Disposable Phaco Pack 3002.P2

GUDID 08717872008929

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

Ophthalmic surgical procedure kit, non-medicated, single-use

• Primary Device ID: 08717872008929
• NIH Device Record Key: 2375f59a-302c-45e2-8e1f-0ab69d876a36
• Commercial Distribution Discontinuation: 2017-07-04
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Disposable Phaco Pack
• Version Model Number: 3002.P2
• Catalog Number: 3002.P2
• Company DUNS: 407522184
• Company Name: D.O.R.C. Dutch Ophthalmic Research Center (International) B.V.
• Device Count: 5
• 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	08717872008929 [Primary]
GS1	18717872008926 [Unit of Use]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K081877

FDA Product Code

• HQC: Unit, Phacofragmentation

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2019-11-08
• Device Publish Date: 2016-09-23

On-Brand Devices [Disposable Phaco Pack]

• 08717872008943: 3002.P4
• 08717872008929: 3002.P2