Armboard

GUDID 07350111830540

Reison Medical AB

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• Primary Device ID: 07350111830540
• NIH Device Record Key: b7a1e619-d85e-4947-a2ac-0c6abce9a0dc
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Armboard
• Version Model Number: 10-380-UK
• Company DUNS: 356766220
• Company Name: Reison 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: true
• Serial Number: false
• 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	07350111830540 [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: 2022-05-09
• Device Publish Date: 2022-04-30

On-Brand Devices [Armboard]

• 07350111832834: 10-380-F-US
• 07350111832827: 10-380-F
• 07350111830717: 10-388-US
• 07350111830700: 10-388-UK
• 07350111830694: 10-388
• 07350111830557: 10-380-US
• 07350111830540: 10-380-UK
• 07350111830533: 10-380-Steris
• 07350111830526: 10-380-S30
• 07350111830519: 10-380-M-US
• 07350111830502: 10-380-M-UK
• 07350111830496: 10-380-M-10
• 07350111830489: 10-380-M
• 07350111830410: 10-380-K-Ergotechnica-2
• 07350111830403: 10-380-K-Ergotechnica
• 07350111830359: 10-380