IGS WF BP

GUDID 00840682141284

GE MEDICAL SYSTEMS

Foot-switch, electrical

• Primary Device ID: 00840682141284
• NIH Device Record Key: a973a8f2-116e-4510-b8e4-699d09d65703
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: IGS WF BP
• Version Model Number: NA
• Company DUNS: 266062561
• Company Name: GE MEDICAL SYSTEMS
• 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: 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00840682141284 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K181403

FDA Product Code

• IZI: System, x-ray, angiographic

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: 2019-07-23
• Device Publish Date: 2019-07-15

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• 00195278719263 - Allia: 2023-12-18 Allia IGS5 UDI
• 00195278719577 - Allia: 2023-12-18 Allia IGS3 UDI
• 00195278719720 - Allia: 2023-12-18 Allia IGS 7 UDI
• 00195278719744 - Allia: 2023-12-18 Allia IGS 7 OR UDI
• 00195278711229 - not applicable: 2023-09-22 UDI Software Pristina