FILM CEPHALOMETRIC

GUDID 00812045030542

FILM CEPHALOMETRIC GREEN SENSITIVE 8 X 10, 100pcs/box

Flow X Ray Corporation

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• Primary Device ID: 00812045030542
• NIH Device Record Key: d94dc785-9eac-425a-b3ea-3dd4cf349ba6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: FILM CEPHALOMETRIC
• Version Model Number: 31101
• Company DUNS: 010016319
• Company Name: Flow X Ray Corporation
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• 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	00812045030542 [Primary]

FDA Product Code

• IWZ: Film, Radiographic

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2023-06-28
• Device Publish Date: 2020-06-01

On-Brand Devices [FILM CEPHALOMETRIC]

• 00812045030559: FILM CEPHALOMETRIC GREEN SENSITIVE 8 X 10, 100pcs/box
• 00812045030542: FILM CEPHALOMETRIC GREEN SENSITIVE 8 X 10, 100pcs/box