Velara R/F 2T 9890-000-70298

GUDID 00884838088542

X-ray control and HV generator

Philips Medical Systems DMC GmbH

Diagnostic x-ray system generator, stationary

• Primary Device ID: 00884838088542
• NIH Device Record Key: b2619f73-c68f-4bfb-a523-32624cbb7d35
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Velara R/F 2T
• Version Model Number: 9890-000-70298
• Catalog Number: 9890-000-70298
• Company DUNS: 314101218
• Company Name: Philips Medical Systems DMC GmbH
• Device Count: 1
• DM Exempt: true
• Pre-market Exempt: true
• 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	00884838088542 [Primary]

FDA Product Code

• IZO: Generator, high-voltage, x-ray, diagnostic

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: 2019-02-11
• Device Publish Date: 2019-01-11

On-Brand Devices [Velara R/F 2T]

• 00884838088542: X-ray control and HV generator
• 00884838076143: X-ray control and HV generator