Treatment Table

GUDID 00850020142262

PIVOTAL HEALTH SOLUTIONS, INC.

Examination/treatment table, manual

• Primary Device ID: 00850020142262
• NIH Device Record Key: cceeae65-188f-4c21-85a5-2c56881c65f2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Treatment Table
• Version Model Number: ET108
• Company DUNS: 826316098
• Company Name: PIVOTAL HEALTH SOLUTIONS, 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: 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	00850020142262 [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: 2021-09-06
• Device Publish Date: 2021-08-27

On-Brand Devices [Treatment Table]

• 00850020142279: ET109
• 00850020142262: ET108
• 00850020142255: ET107
• 00850020142248: ET106
• 00850020142231: Non-electric, fixed height model in the ET series of treatment cabinets with an open shelf.