ENDOMAT

GUDID 04048551066423

ENDOMAT® LC SCB, Roller Pump

Karl Storz GmbH & Co. KG

Surgical suction system

• Primary Device ID: 04048551066423
• NIH Device Record Key: 04af9dec-1e35-4c1a-b8fb-3410aace79df
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ENDOMAT
• Version Model Number: 20330320-1
• Company DUNS: 315731430
• Company Name: Karl Storz GmbH & Co. KG
• 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	04048551066423 [Primary]

FDA Product Code

• OCX: endoscopic irrigation/suction system

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: 2024-10-21
• Device Publish Date: 2016-09-23

On-Brand Devices [ENDOMAT]

• 04048551376041: ENDOMAT SELECT
• 04048551066423: ENDOMAT® LC SCB, Roller Pump