Backflush Instrument with 20 gauge / 0.9 mm brush needle. 2281.BD

GUDID 18717872026142

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

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• Primary Device ID: 18717872026142
• NIH Device Record Key: 3105bee7-5f76-462f-a1f8-693834bb6231
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Backflush Instrument with 20 gauge / 0.9 mm brush needle.
• Version Model Number: 2281.BD
• Catalog Number: 2281.BD
• 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: 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	08717872026145 [Primary]
GS1	18717872026142 [Unit of Use]

FDA Product Code

• HMX: Cannula, Ophthalmic

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2021-02-24
• Device Publish Date: 2021-02-11

On-Brand Devices [Backflush Instrument with 20 gauge / 0.9 mm brush needle.]

• 18717872018611: 2281.BD
• 18717872026142: 2281.BD