VITOM

GUDID 04048551387733

VITOM® 3D Illuminator

Karl Storz GmbH & Co. KG

Fixed examination/treatment room light

• Primary Device ID: 04048551387733
• NIH Device Record Key: 1a674671-1930-4b70-af3f-0894edb77bba
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VITOM
• Version Model Number: TH002
• Company DUNS: 315731430
• Company Name: Karl Storz 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: true
• Serial Number: false
• Manufacturing Date: false
• 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	04048551387733 [Primary]

FDA Product Code

• EPT: MICROSCOPE, SURGICAL

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: 2021-01-08
• Device Publish Date: 2018-07-21

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• 04048551387733: VITOM® 3D Illuminator