Insight 138017

GUDID 00817517026900

Insight GynoCart with Exam Light

MARKETLAB INC.

Examination/operating table component trolley

• Primary Device ID: 00817517026900
• NIH Device Record Key: 5362933f-a378-4806-a3a1-f1a28d23520d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Insight
• Version Model Number: 138017
• Catalog Number: 138017
• Company DUNS: 848917027
• Company Name: MARKETLAB INC.
• 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: true
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00817517026900 [Primary]

FDA Product Code

• LGX: Table, Examination, Medical, 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: 2023-09-18
• Device Publish Date: 2023-09-08

On-Brand Devices [Insight]

• 00817517026900: Insight GynoCart with Exam Light
• 00817517026894: Insight GynoCart Exam Cart