Sim.LED 350 3p

GUDID 04250613838910

S.I.M.E.O.N. Medical GmbH & Co. KG

Fixed examination/treatment light Fixed examination/treatment room light Fixed examination/treatment room light Fixed examination/treatment room light Fixed examination/treatment room light Fixed examination/treatment room light Fixed examination/treatment room light Fixed examination/treatment room light Fixed examination/treatment room light Fixed examination/treatment room light Fixed examination/treatment room light Fixed examination/treatment room light Fixed examination/treatment room light Fixed examination/treatment room light Fixed examination/treatment room light

• Primary Device ID: 04250613838910
• NIH Device Record Key: 88291c77-c913-4d65-8dd9-24681818cf03
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Sim.LED 350 3p
• Version Model Number: 141-0015725
• Company DUNS: 344838128
• Company Name: S.I.M.E.O.N. Medical GmbH & Co. KG
• 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	04250613838910 [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: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2018-10-05
• Device Publish Date: 2018-09-04

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