Extendible 41 G subretinal injection needle. (23 gauge / 0.6 mm) 1270.EXT

GUDID 18717872002092

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

Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use

• Primary Device ID: 18717872002092
• NIH Device Record Key: bddf4b6d-dee0-4d59-b010-5beb1d3a01ef
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Extendible 41 G subretinal injection needle. (23 gauge / 0.6 mm)
• Version Model Number: 1270.EXT
• Catalog Number: 1270.EXT
• 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	08717872002095 [Primary]
GS1	18717872002092 [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: 2021-02-19
• Device Publish Date: 2021-02-01

On-Brand Devices [Extendible 41 G subretinal injection needle. (23 gauge / 0.6 mm)]

• 18717872002108: 1270.EXT
• 18717872002092: 1270.EXT