Sonesta

GUDID 07350006950056

Sonesta Medical AB

Examination/treatment table, line-powered

• Primary Device ID: 07350006950056
• NIH Device Record Key: 50862eff-bbed-413c-b318-7f1e56ddb0c3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Sonesta
• Version Model Number: SST
• Company DUNS: 355118308
• Company Name: Sonesta Medical AB
• 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	07350006950056 [Primary]

FDA Product Code

• IXR: Table, Radiographic, Tilting

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: 2019-06-24
• Device Publish Date: 2019-06-14

On-Brand Devices [Sonesta]

• 00735000695003: S3
• 07350006950025: S2
• 07350006950018: 6210
• 07350006950032: S3
• 07350006950056: SST