DU 33100 DA 90 HS 9890-000-85611

GUDID 00884838076242

diagnostic x-ray tube housing assembly

Philips Medical Systems DMC GmbH

X-ray tube housing assembly, diagnostic

• Primary Device ID: 00884838076242
• NIH Device Record Key: 8d9b1893-fc94-495a-9487-4c5e66f99ad2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DU 33100 DA 90 HS
• Version Model Number: 9890-000-85611
• Catalog Number: 9890-000-85611
• 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	00884838076242 [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

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