XS-100 X-Ray Tube Assembly 301001

GUDID 00884838113749

Diagnostic x-ray tube housing assembly

Philips Medical Systems DMC GmbH

X-ray tube housing assembly, diagnostic

• Primary Device ID: 00884838113749
• NIH Device Record Key: 04d003e1-9b5e-47c6-9aef-f237d1efd1e3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: XS-100 X-Ray Tube Assembly
• Version Model Number: 301001
• Catalog Number: 301001
• 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	00884838113749 [Primary]

FDA Product Code

• ITY: Assembly, tube housing, 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: 2023-09-08
• Device Publish Date: 2023-08-31

On-Brand Devices [XS-100 X-Ray Tube Assembly]

• 00884838083455: diagnostic x-ray tube housing assembly
• 00884838070868: diagnostic x-ray tube housing assembly
• 00884838103641: diagnostic x-ray tube housing assembly
• 00884838103634: diagnostic x-ray tube housing assembly
• 00884838108158: diagnostic x-ray tube housing assembly
• 00884838107243: diagnostic x-ray tube housing assembly
• 00884838113749: Diagnostic x-ray tube housing assembly