Euflexxa

GUDID 54158041000006

9902392 Canada Inc

Synovial fluid supplementation medium

• Primary Device ID: 54158041000006
• NIH Device Record Key: d04c8cee-7b92-4360-89b4-2ed7abc48cfb
• Commercial Distribution Discontinuation: 2017-02-28
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Euflexxa
• Version Model Number: 024
• Company DUNS: 203324624
• Company Name: 9902392 Canada Inc
• Device Count: 1
• 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

Customer Support Contacts

• Phone: 999-999-9999
• Email: info@export.ooo
• Phone: 999-999-9999
• Email: info@export.ooo

Device Identifiers

Device Issuing Agency	Device ID
GS1	54158041000006 [Primary]

FDA Product Code

• MOZ: Acid, Hyaluronic, Intraarticular

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-07-09
• Device Publish Date: 2016-12-05

On-Brand Devices [Euflexxa]

• 00627843737810: 024
• 54158041000006: 024