Replacement backflush needle, straight 23G / 0.6 mm for 1281.C backflush handpie 1281.A5D06

GUDID 18717872003518

Replacement backflush needle, straight 23G / 0.6 mm for 1281.C backflush handpiece

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

Vitrectomy fluid/gas handling handpiece/cannula Vitrectomy fluid/gas handling handpiece/cannula Vitrectomy fluid/gas handling handpiece/cannula Vitrectomy fluid/gas handling handpiece/cannula Vitrectomy fluid/gas handling handpiece/cannula Vitrectomy fluid/gas handling handpiece/cannula Vitrectomy fluid/gas handling handpiece/cannula Vitrectomy fluid/gas handling handpiece/cannula Vitrectomy fluid/gas handling handpiece/cannula Vitrectomy fluid/gas handling handpiece/cannula Vitrectomy fluid/gas handling handpiece/cannula Vitrectomy fluid/gas handling handpiece/cannula Vitrectomy fluid/gas handling handpiece/cannula Vitrectomy fluid/gas handling handpiece/cannula Vitrectomy fluid/gas handling handpiece/cannula Vitrectomy fluid/gas handling handpiece/cannula

• Primary Device ID: 18717872003518
• NIH Device Record Key: ae183da0-5f76-46c1-b6c1-4bf7352b81c5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Replacement backflush needle, straight 23G / 0.6 mm for 1281.C backflush handpie
• Version Model Number: 1281.A5D06
• Catalog Number: 1281.A5D06
• Company DUNS: 407522184
• Company Name: D.O.R.C. Dutch Ophthalmic Research Center (International) B.V.
• Device Count: 10
• 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	08717872003511 [Primary]
GS1	18717872003518 [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: 2021-02-22
• Device Publish Date: 2020-11-16

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