MICROCAST

GUDID 04048551318218

Microcast® HD Studio CCU

Karl Storz GmbH & Co. KG

Endoscopic video image processing unit

• Primary Device ID: 04048551318218
• NIH Device Record Key: 019f341e-76d3-4b8f-8df5-cb489c91f4d4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MICROCAST
• Version Model Number: 20960300
• Company DUNS: 315731430
• Company Name: Karl Storz GmbH & Co. KG
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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	04048551318218 [Primary]

FDA Product Code

• EPT: MICROSCOPE, SURGICAL

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2020-05-19
• Device Publish Date: 2019-02-23

On-Brand Devices [MICROCAST]

• 04048551356616: Microcast® HD Pro-Lite Set, Cable 900 cm
• 04048551318232: Microcast® HD Pro-Lite CCU
• 04048551318218: Microcast® HD Studio CCU