CT4000 9890-000-87501

GUDID 00884838105454

diagnostic x-ray tube housing assembly

Philips Medical Systems DMC GmbH

X-ray tube housing assembly, diagnostic

• Primary Device ID: 00884838105454
• NIH Device Record Key: 00dafba5-c514-4d6a-8076-077325a020a9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CT4000
• Version Model Number: 9890-000-87501
• Catalog Number: 9890-000-87501
• 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	00884838105454 [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