Tradeflex Flexion Table

GUDID 00850008449895

PIVOTAL HEALTH SOLUTIONS, INC.

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• Primary Device ID: 00850008449895
• NIH Device Record Key: 07fed5df-454e-43b8-b7de-75d12b7b5fee
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Tradeflex Flexion Table
• Version Model Number: E9217
• 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	00850008449895 [Primary]

FDA Product Code

• INQ: Table, Powered

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 [Tradeflex Flexion Table]

• 00850008449925: E9218-L
• 00850008449918: E9218
• 00850008449901: E9217-L
• 00850008449895: E9217
• 00850008449888: E9018-L
• 00850008449871: E9018
• 00850008449864: E9017-L
• 00850008449857: E9017