CTR2250 9896-055-92411

GUDID 00884838092181

diagnostic x-ray tube housing assembly

Philips Medical Systems DMC GmbH

X-ray tube housing assembly, diagnostic

• Primary Device ID: 00884838092181
• NIH Device Record Key: 735b5d93-cd68-417a-a492-37dabbf11da2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CTR2250
• Version Model Number: 9896-055-92411
• Catalog Number: 9896-055-92411
• 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	00884838092181 [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: 2019-02-11
• Device Publish Date: 2019-01-11

On-Brand Devices [CTR2250]

• 00884838092839: diagnostic x-ray tube housing assembly
• 00884838092464: diagnostic x-ray tube housing assembly
• 00884838092457: diagnostic x-ray tube housing assembly
• 00884838092440: diagnostic x-ray tube housing assembly
• 00884838092433: diagnostic x-ray tube housing assembly
• 00884838092389: diagnostic x-ray tube housing assembly
• 00884838092372: diagnostic x-ray tube housing assembly
• 00884838092181: diagnostic x-ray tube housing assembly