Dental X-Ray Company

GUDID 08052870660213

DENTAL XRAY COMPANY SRL

Stationary intraoral dental x-ray system, analogue

• Primary Device ID: 08052870660213
• NIH Device Record Key: 6283d46f-4d32-4a7d-8b5f-4d6fdea8ecd7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Dental X-Ray Company
• Version Model Number: Endograph DC
• Company DUNS: 439922846
• Company Name: DENTAL XRAY COMPANY SRL
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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	08052870660213 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K130109

FDA Product Code

• EHD: Unit, X-Ray, Extraoral With Timer

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: 2019-07-09
• Device Publish Date: 2019-07-01

On-Brand Devices [Dental X-Ray Company]

• 08052870660619: Explor-X ACP
• 08052870660510: Explor-X AC
• 08052870660411: Endos ACP
• 08052870660312: Endos AC
• 08052870660213: Endograph DC