KARL STORZ AIDA

GUDID 04048551012901

KARL STORZ AIDA 2.0 HL7

Karl Storz GmbH & Co. KG

Operating room audiovisual data/device management system application software

• Primary Device ID: 04048551012901
• NIH Device Record Key: 1ba23427-1b31-4fea-b96b-742fc8cbde64
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: KARL STORZ AIDA
• Version Model Number: 20040021-V01
• 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: false
• 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	04048551012901 [Primary]

FDA Product Code

• FET: Endoscopic video imaging system/component, gastroenterology-urology

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 [KARL STORZ AIDA]

• 04048551356388: AIDA DVD-M HD Kit, DOMESTIC, CE
• 04048551405734: AIDA 2.0 Office 10 licences
• 04048551012901: KARL STORZ AIDA 2.0 HL7
• 04048551012888: AIDA 2.0 Office Software