Upper Cervical Store

GUDID 00628942541612

Fixed Table

Upper Cervical Store Inc

Examination/treatment table, line-powered

• Primary Device ID: 00628942541612
• NIH Device Record Key: 0a88a229-4553-4257-8d40-37c3d3980b3e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Upper Cervical Store
• Version Model Number: FT
• Company DUNS: 241897748
• Company Name: Upper Cervical Store Inc
• 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: false
• Manufacturing Date: false
• 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	00628942541612 [Primary]

FDA Product Code

• INW: Table, Mechanical

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: 2024-02-08
• Device Publish Date: 2024-01-31

On-Brand Devices [Upper Cervical Store]

• 00628942541605: Elevating Table
• 00628942541612: Fixed Table