Xenon Light Source

GUDID 04056702003234

W.O.M. World of Medicine GmbH

Endoscopic light source, line-powered

• Primary Device ID: 04056702003234
• NIH Device Record Key: bd795073-e0d6-449b-9c48-0c0fcd5f0da6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Xenon Light Source
• Version Model Number: XL300
• Company DUNS: 316305242
• Company Name: W.O.M. World of Medicine GmbH
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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	04056702003234 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K021717

FDA Product Code

• GCT: Light Source, Endoscope, Xenon Arc

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-02-21
• Device Publish Date: 2016-08-09

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