XLinearVision

GUDID 06972259248042

Shenzhen Xpectvision Technology Co.,Ltd.

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• Primary Device ID: 06972259248042
• NIH Device Record Key: 99b526a6-cebe-4db1-9958-05694c922d22
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: XLinearVision
• Version Model Number: XVC001/XVC002/XVC003/XVC004
• Company DUNS: 560445687
• Company Name: Shenzhen Xpectvision Technology Co.,Ltd.
• 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: false
• Serial Number: true
• Manufacturing Date: true
• 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	06972259248042 [Primary]

FDA Product Code

• NRU: Chair, Dental, Without Operative Unit

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: 2022-11-21
• Device Publish Date: 2022-11-11

On-Brand Devices [XLinearVision]

• 06972259248011: XVD2530
• 06972259248004: XVD2121 Plus
• 06972259248035: XVH001
• 06972259248042: XVC001/XVC002/XVC003/XVC004