uOmnispace

GUDID 06971576834259

Shanghai United Imaging Healthcare Co., Ltd.

MRI system application software

• Primary Device ID: 06971576834259
• NIH Device Record Key: a53ad32e-6042-4f47-b69a-8a0aff13ca0c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: uOmnispace
• Version Model Number: uOmnispace.MR
• Company DUNS: 421271328
• Company Name: Shanghai United Imaging Healthcare Co., Ltd.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(855) 221-1552
• Email: CustomerSuccess@united-imaging.com
• Phone: +1(855) 221-1552
• Email: CustomerSuccess@united-imaging.com
• Phone: +1(855) 221-1552
• Email: CustomerSuccess@united-imaging.com
• Phone: +1(855) 221-1552
• Email: CustomerSuccess@united-imaging.com
• Phone: +1(855) 221-1552
• Email: CustomerSuccess@united-imaging.com
• Phone: +1(855) 221-1552
• Email: CustomerSuccess@united-imaging.com
• Phone: +1(855) 221-1552
• Email: CustomerSuccess@united-imaging.com
• Phone: +1(855) 221-1552
• Email: CustomerSuccess@united-imaging.com
• Phone: +1(855) 221-1552
• Email: CustomerSuccess@united-imaging.com
• Phone: +1(855) 221-1552
• Email: CustomerSuccess@united-imaging.com
• Phone: +1(855) 221-1552
• Email: CustomerSuccess@united-imaging.com
• Phone: +1(855) 221-1552
• Email: CustomerSuccess@united-imaging.com
• Phone: +1(855) 221-1552
• Email: CustomerSuccess@united-imaging.com
• Phone: +1(855) 221-1552
• Email: CustomerSuccess@united-imaging.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	06971576834259 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K233186

FDA Product Code

• QIH: Automated Radiological Image Processing Software

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: 2025-08-11
• Device Publish Date: 2025-08-02

On-Brand Devices [uOmnispace]

• 06971576834259: uOmnispace.MR
• 06971576834242: uOmnispace.MI
• 06971576834228: uOmnispace
• 06971576834204: uOmnispace.CT