CT8000 9806-058-01431

GUDID 00884838107229

diagnostic x-ray tube housing assembly

Philips Medical Systems DMC GmbH

X-ray tube housing assembly, diagnostic X-ray tube housing assembly, diagnostic X-ray tube housing assembly, diagnostic X-ray tube housing assembly, diagnostic X-ray tube housing assembly, diagnostic X-ray tube housing assembly, diagnostic X-ray tube housing assembly, diagnostic X-ray tube housing assembly, diagnostic

• Primary Device ID: 00884838107229
• NIH Device Record Key: 2c3a9a1a-b017-4e6b-a4b4-4c0ca39bcddf
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CT8000
• Version Model Number: 9806-058-01431
• Catalog Number: 9806-058-01431
• 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	00884838107229 [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: 2021-08-02
• Device Publish Date: 2021-07-25

On-Brand Devices [CT8000]

• 00884838091795: diagnostic x-ray tube housing assembly
• 00884838093126: diagnostic x-ray tube housing assembly
• 00884838093119: diagnostic x-ray tube housing assembly
• 00884838103658: diagnostic x-ray tube housing assembly
• 00884838108189: diagnostic x-ray tube housing assembly
• 00884838107229: diagnostic x-ray tube housing assembly