invendo ScopeController

GUDID 04260444390051

invendo medical GmbH

Endoscopic control/video-imaging system

• Primary Device ID: 04260444390051
• NIH Device Record Key: 05d72804-fe49-40ce-bd46-d387c57ef887
• Commercial Distribution Discontinuation: 2019-06-18
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: invendo ScopeController
• Version Model Number: SCCV1
• 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: false
• Lot Batch: false
• Serial Number: true
• 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	04260444390051 [Primary]

FDA Product Code

• FDF: Colonoscope And Accessories, Flexible/Rigid

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: 2019-06-19
• Device Publish Date: 2016-09-22

Devices Manufactured by invendo medical GmbH

• 04260444390051 - invendo ScopeController: 2019-06-19
• 04260444390051 - invendo ScopeController: 2019-06-19
• 04260444390075 - invendo SPU Processing Unit: 2019-06-19
• 04260444390082 - invendo SPU Power Unit: 2019-06-19
• 04260444390112 - invendoscope: 2019-06-19
• 04260444390013 - invendoscope: 2019-02-21
• 04260444390037 - invendo SPU Processing Unit: 2019-02-21
• 04260444390044 - invendo SPU Power Unit: 2019-02-21