CIRCLED 110002

GUDID 08050705890026

CIRCLED 3/5 DIOPTERS WALL

ACEM SPA

Fixed examination/treatment light

• Primary Device ID: 08050705890026
• NIH Device Record Key: 3f56cd26-cf3e-4590-ae46-5756ffb0e7a4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CIRCLED
• Version Model Number: CIRCLED /W
• Catalog Number: 110002
• 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	08050705890026 [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 [CIRCLED]

• 08050705890033: CIRCLED 3/5 DIOPTERS TROLLEY
• 08050705890026: CIRCLED 3/5 DIOPTERS WALL
• 08050705890019: CIRCLED 3/5 DIOPTERS TABLE
• 08050705890002: CIRCLED 3/5 DIOPTERS RAIL