VidiaPort

GUDID 00887761968523

VidiaPort Ceiling Single

TRUMPF Medizin Systeme GmbH + Co. KG

Operating room light system Operating room light system Operating room light system Operating room light system Operating room light system Operating room light system

• Primary Device ID: 00887761968523
• NIH Device Record Key: 8785fee9-1f51-428a-ae09-db37fe995ca8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VidiaPort
• Version Model Number: 4028110
• Company DUNS: 330961223
• Company Name: TRUMPF Medizin Systeme 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

Customer Support Contacts

• Phone: +4936715860
• Email: SURGICAL@HILLROM.COM
• Phone: +4936715860
• Email: SURGICAL@HILLROM.COM
• Phone: +4936715860
• Email: SURGICAL@HILLROM.COM
• Phone: +4936715860
• Email: SURGICAL@HILLROM.COM
• Phone: +4936715860
• Email: SURGICAL@HILLROM.COM
• Phone: +4936715860
• Email: SURGICAL@HILLROM.COM

Device Identifiers

Device Issuing Agency	Device ID
GS1	00887761968523 [Primary]

FDA Product Code

• KQM: CAMERA, SURGICAL AND ACCESSORIES

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: 2023-01-13
• Device Publish Date: 2023-01-05

On-Brand Devices [VidiaPort]

• 00887761968523: VidiaPort Ceiling Single
• 00887761968462: VidiaPort Ceiling Duo
• 00887761968455: VidiaPort Ceiling Trio