Aspiration cannula

GUDID 04059082031507

SOPRO-COMEG GmbH

Endoscopic irrigation/aspiration pump

• Primary Device ID: 04059082031507
• NIH Device Record Key: 98ac9a7c-4c10-4b56-bc9b-c0402fbf018d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Aspiration cannula
• Version Model Number: 195 200 230
• 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	04059082031507 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K971881

FDA Product Code

• FDC: RESECTOSCOPE, WORKING ELEMENT

Sterilization

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

[04059082031507]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-07-06
• Device Publish Date: 2018-03-20

On-Brand Devices [Aspiration cannula]

• 04059082031538: 195 200 270
• 04059082031507: 195 200 230
• 04059082009490: 195 200 270BC
• 04059082009469: 195 200 230BC