Inflow cannula

GUDID 04059082033242

SOPRO-COMEG GmbH

Suction cannula, reusable

• Primary Device ID: 04059082033242
• NIH Device Record Key: 197c99c8-81e5-45aa-93a7-97e25af0a4d7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Inflow cannula
• Version Model Number: 191 501 600
• Company DUNS: 507185952
• Company Name: SOPRO-COMEG 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: true
• 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	04059082033242 [Primary]

FDA Product Code

• HRX: Arthroscope

Sterilization

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

[04059082033242]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2018-04-20
• Device Publish Date: 2018-03-20

On-Brand Devices [Inflow cannula]

• 04059082033259: 191 501 603
• 04059082033242: 191 501 600
• 04059082007830: 191 501 603
• 04059082007809: 191 501 600