DYEVERT™ NG

GUDID 00815241020089

CONTRAST MODULATION SYSTEM

OSPREY MEDICAL INC.

Contrast medium conservation system

• Primary Device ID: 00815241020089
• NIH Device Record Key: 40a59932-9af8-4898-a8f9-d847075ca885
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DYEVERT™ NG
• Version Model Number: LVOFF
• Company DUNS: 938215568
• Company Name: OSPREY MEDICAL INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Safe
• 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: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 9529558247
• Email: vfabano@ospreymed.com
• Phone: 9529558247
• Email: vfabano@ospreymed.com
• Phone: 9529558247
• Email: vfabano@ospreymed.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00815241020089 [Primary]

FDA Product Code

• DXT: Injector And Syringe, Angiographic

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: 2018-03-29
• Device Publish Date: 2016-09-12

On-Brand Devices [DYEVERT™ NG ]

• 00815241020089: CONTRAST MODULATION SYSTEM
• 00815241020072: CONTRAST MODULATION SYSTEM