Eagle Vision DCR Stent 1087

GUDID 00841668114872

DCR Intubation Set 40mm L x .79mm OD - 1 per box

KATENA PRODUCTS, INC.

Lacrimal procedural cannula

• Primary Device ID: 00841668114872
• NIH Device Record Key: 49780f6f-2ba6-47f3-9963-587edcad9713
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Eagle Vision DCR Stent
• Version Model Number: 1087
• Catalog Number: 1087
• Company DUNS: 085668598
• Company Name: KATENA PRODUCTS, INC.
• Device Count: 1
• DM Exempt: true
• 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

Customer Support Contacts

• Phone: (973) 989-1600
• Email: globe@katena.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00841668114872 [Primary]

FDA Product Code

• OKS: Lacrimal Stents And Intubation Sets

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2019-12-11
• Device Publish Date: 2017-03-31

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