invendoscope

GUDID 04260444390013

invendo medical GmbH

Flexible video colonoscope, single-use

• Primary Device ID: 04260444390013
• NIH Device Record Key: 964e5311-4f05-47af-8712-b1bdb7dbb590
• Commercial Distribution Discontinuation: 2017-11-30
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: invendoscope
• Version Model Number: SC200
• Company DUNS: 333191497
• Company Name: invendo medical 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: true
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: false
• Expiration Date: true
• 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	04260444390013 [Primary]
GS1	04260444390020 [Package]; Package: [5 Units]; Discontinued: 2017-11-30; Not in Commercial Distribution

FDA Product Code

• FDF: Colonoscope And Accessories, Flexible/Rigid

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-02-21
• Device Publish Date: 2016-09-22

On-Brand Devices [invendoscope ]

• 04260444390112: SC210
• 04260444390013: SC200