Philips 459800766651

GUDID 00884838089631

dS FootAnkle Coil 8ch 1.5T

Philips Ds North America LLC

MRI system coil, radio-frequency

• Primary Device ID: 00884838089631
• NIH Device Record Key: 8dd829d4-ae45-4511-bfbd-746798886b22
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Philips
• Version Model Number: dS FootAnkle Coil 8ch 1.5T
• Catalog Number: 459800766651
• Company DUNS: 009237140
• Company Name: Philips Ds North America LLC
• 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: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00884838089631 [Primary]

FDA Product Code

• MOS: Coil, Magnetic Resonance, Specialty

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: 2025-12-31
• Device Publish Date: 2025-12-23

On-Brand Devices [Philips]

• 00884838117952: ds KNEE 8Ch 3.0T
• 00884838089631: dS FootAnkle Coil 8ch 1.5T
• 00884838089624: dS Wrist Coil 8ch 1.5T