X-Ray Grid 60/10/140

GUDID 00884838125469

Philips Medical Systems DMC GmbH

Stationary x-ray grid

• Primary Device ID: 00884838125469
• NIH Device Record Key: c6a1f417-e7a4-44db-9342-8c42249e299b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: X-Ray Grid 60/10/140
• Version Model Number: 9896-010-64292
• 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	00884838125469 [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 60/10/140]

• 00884838074408: 9896-010-64291
• 00884838125469: 9896-010-64292