EVA Vitrectomy Pack Gravity Input 23G 8300.23G01

GUDID 08717872018997

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

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

• Primary Device ID: 08717872018997
• NIH Device Record Key: bfe857e1-92ec-476f-b9d5-4054eebb11cf
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: EVA Vitrectomy Pack Gravity Input 23G
• Version Model Number: 8300.23G01
• Catalog Number: 8300.23G01
• 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	08717872018997 [Primary]
GS1	18717872018994 [Unit of Use]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K190875

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: 6
• Public Version Date: 2020-03-19
• Device Publish Date: 2016-09-23

On-Brand Devices [EVA Vitrectomy Pack Gravity Input 23G]

• 08717872030685: 8300.23G11
• 08717872018997: 8300.23G01