SOLED15-F 110403

GUDID 08050705890323

SOLED15-F TROLLEY

ACEM SPA

Mobile examination/treatment light

• Primary Device ID: 08050705890323
• NIH Device Record Key: 01c2cda0-5b6d-409f-b215-a3bad9ff237b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SOLED15-F
• Version Model Number: SOLED15-F /T
• Catalog Number: 110403
• Company DUNS: 435188508
• Company Name: ACEM SPA
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	08050705890323 [Primary]

FDA Product Code

• KZF: Device, Medical Examination, Ac Powered

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2020-03-20
• Device Publish Date: 2020-01-31

On-Brand Devices [SOLED15-F]

• 08050705890354: SOLED15-F 2-ARM CEILING STANDARD LINE
• 08050705890347: SOLED15-F 1-ARM CEILING STANDARD LINE
• 08050705890330: SOLED15-F TROLLEY ABPS
• 08050705890323: SOLED15-F TROLLEY
• 08050705890316: SOLED15-F WALL