PPG Finger Band 3941-02-15

GUDID 00816396023291

PPG Finger Band

IVY BIOMEDICAL SYSTEMS, INC.

MRI system synchronizer

• Primary Device ID: 00816396023291
• NIH Device Record Key: b00d87c3-91c9-4de3-a320-00d99a21b97f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PPG Finger Band
• Version Model Number: 3941-02-15
• Catalog Number: 3941-02-15
• Company DUNS: 109132019
• Company Name: IVY BIOMEDICAL SYSTEMS, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Conditional
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: false
• 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: 203-481-4183
• Email: sales@ivybiomedical.com
• Phone: 203-481-4183
• Email: sales@ivybiomedical.com
• Phone: 203-481-4183
• Email: sales@ivybiomedical.com
• Phone: 203-481-4183
• Email: sales@ivybiomedical.com
• Phone: 203-481-4183
• Email: sales@ivybiomedical.com
• Phone: 203-481-4183
• Email: sales@ivybiomedical.com
• Phone: 203-481-4183
• Email: sales@ivybiomedical.com
• Phone: 203-481-4183
• Email: sales@ivybiomedical.com
• Phone: 203-481-4183
• Email: sales@ivybiomedical.com
• Phone: 203-481-4183
• Email: sales@ivybiomedical.com
• Phone: 203-481-4183
• Email: sales@ivybiomedical.com
• Phone: 203-481-4183
• Email: sales@ivybiomedical.com
• Phone: 203-481-4183
• Email: sales@ivybiomedical.com
• Phone: 203-481-4183
• Email: sales@ivybiomedical.com
• Phone: 203-481-4183
• Email: sales@ivybiomedical.com
• Phone: 203-481-4183
• Email: sales@ivybiomedical.com
• Phone: 203-481-4183
• Email: sales@ivybiomedical.com

Device Dimensions

• Lumen/Inner Diameter: 35 Millimeter
• Lumen/Inner Diameter: 35 Millimeter
• Lumen/Inner Diameter: 35 Millimeter
• Lumen/Inner Diameter: 35 Millimeter
• Lumen/Inner Diameter: 35 Millimeter
• Lumen/Inner Diameter: 35 Millimeter
• Lumen/Inner Diameter: 35 Millimeter
• Lumen/Inner Diameter: 35 Millimeter
• Lumen/Inner Diameter: 35 Millimeter
• Lumen/Inner Diameter: 35 Millimeter
• Lumen/Inner Diameter: 35 Millimeter
• Lumen/Inner Diameter: 35 Millimeter
• Lumen/Inner Diameter: 35 Millimeter
• Lumen/Inner Diameter: 35 Millimeter
• Lumen/Inner Diameter: 35 Millimeter
• Lumen/Inner Diameter: 35 Millimeter
• Lumen/Inner Diameter: 35 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00816396023291 [Primary]

FDA Product Code

• LNH: System, Nuclear Magnetic Resonance Imaging

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-06-16
• Device Publish Date: 2023-06-08

On-Brand Devices [PPG Finger Band]

• 00816396022805: PPG Finger Band
• 00816396022799: PPG Finger Band
• 00816396022782: PPG Finger Band
• 00816396022775: PPG Finger Band
• 00816396022768: PPG Finger Band
• 00816396022751: PPG Finger Band
• 00816396023307: PPG Finger Band
• 00816396023291: PPG Finger Band
• 00816396023284: PPG Finger Band
• 00816396023277: PPG Finger Band
• 00816396023260: PPG Finger Band