CT4000 304031

GUDID 00884838121386

Diagnostic x-ray tube housing assembly

Philips Medical Systems DMC GmbH

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• Primary Device ID: 00884838121386
• NIH Device Record Key: c33a4b73-07fa-4615-911c-993ca39625a2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CT4000
• Version Model Number: 304031
• Catalog Number: 304031
• 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	00884838121386 [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 [CT4000]

• 00884838105430: diagnostic x-ray tube housing assembly
• 00884838121386: Diagnostic x-ray tube housing assembly
• 00884838105454: diagnostic x-ray tube housing assembly