Nephroscopy obturator

GUDID 04059082009612

SOPRO-COMEG GmbH

Rigid endoscope obturator

• Primary Device ID: 04059082009612
• NIH Device Record Key: 4e78ed3b-45d1-4a9e-8004-fd1c353488dc
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Nephroscopy obturator
• Version Model Number: 195 800 020BC
• 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: false
• 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	04059082009612 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K945262

FDA Product Code

• FAJ: Cystoscope and accessories, flexible/rigid

Sterilization

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

[04059082009612]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-12-22

On-Brand Devices [Nephroscopy obturator]

• 04059082030104: 195 800 020
• 04059082009612: 195 800 020BC