GoECG

GUDID 04251341900245

CORSCIENCE GmbH & Co. KG

Electrocardiograph, professional, multichannel

• Primary Device ID: 04251341900245
• NIH Device Record Key: c08de0c6-f141-4d6d-accb-4e5debdcc0d4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: GoECG
• Version Model Number: CS10785-08
• Company DUNS: 333427776
• Company Name: CORSCIENCE 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	04251341900245 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K183369

FDA Product Code

• DPS: Electrocardiograph

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-03-11
• Device Publish Date: 2019-02-11

On-Brand Devices [GoECG]

• 04251341900245: CS10785-08
• 04251341900238: CS10785-07