UltraScan Versa

GUDID 00848871001395

UltraScan Versa, H-F, Calf, Stirrup

MEDICAL POSITIONING, INC.

Multi-purpose diagnostic imaging table

• Primary Device ID: 00848871001395
• NIH Device Record Key: fbc65d6d-c4da-4a2e-97e6-0fee2e44e865
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: UltraScan Versa
• Version Model Number: 087-C
• Company DUNS: 803035633
• Company Name: MEDICAL POSITIONING, 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: 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

Customer Support Contacts

• Phone: 816-595-2359
• Email: productsupport@medicalpositioning.com
• Phone: 816-595-2359
• Email: productsupport@medicalpositioning.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00848871001395 [Primary]

FDA Product Code

• LGX: Table, Examination, Medical, 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: 2020-10-19
• Device Publish Date: 2020-10-09

On-Brand Devices [UltraScan Versa]

• 00848871001326: UltraScan Versa, H-F-T, Calf, Stirrup, 2AD
• 00848871001319: UltraScan Versa, H-F, Calf, Stirrup, 2AD
• 00848871001302: UltraScan Versa, H-F-T, Calf, Stirrup, 2D
• 00848871001296: UltraScan Versa, H-F, Calf, Stirrup, 2D
• 00848871001289: UltraScan Versa, H-F-T, Calf, Stirrup
• 00848871001272: UltraScan Versa, H-F-T, Calf, Stirrup, Footboard
• 00848871001265: UltraScan Versa, H-F, Calf, Stirrup
• 00848871001395: UltraScan Versa, H-F, Calf, Stirrup