X-Ray Grid 36/12/100

GUDID 00884838125582

Philips Medical Systems DMC GmbH

Stationary x-ray grid

• Primary Device ID: 00884838125582
• NIH Device Record Key: 26e37ff5-65ca-4603-b391-65a17ba128b0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: X-Ray Grid 36/12/100
• Version Model Number: 9896-010-61302
• Company DUNS: 314101218
• Company Name: Philips Medical Systems DMC GmbH
• Device Count: 1
• DM Exempt: false
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00884838125582 [Primary]

FDA Product Code

• IXJ: Grid, Radiographic

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: 2025-06-27
• Device Publish Date: 2025-06-19

On-Brand Devices [X-Ray Grid 36/12/100 ]

• 00884838095106: 9896-010-61301
• 00884838125582: 9896-010-61302