ECG Cable for CM 3000-12 BT / SEER 12 10 Leads 2014606-635

GUDID 04250903201172

The cable is intended to be used to conduct electrical signals from a patient's heart, via an electrode attached to the surface of the chest/limbs, to

getemed Medizin- und Informationstechnik AG

Electrocardiographic lead set, reusable

• Primary Device ID: 04250903201172
• NIH Device Record Key: 685fc301-bb68-40bc-baa6-3112c9b84ece
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ECG Cable for CM 3000-12 BT / SEER 12 10 Leads
• Version Model Number: 130 cm, IEC Color Code, Round
• Catalog Number: 2014606-635
• Company DUNS: 331682898
• Company Name: getemed Medizin- und Informationstechnik AG
• 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: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: true
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +49332939420
• Email: info@getemed.de

Operating and Storage Conditions

• Storage Environment Humidity: Between 0 Percent (%) Relative Humidity and 90 Percent (%) Relative Humidity
• Storage Environment Temperature: Between -25 Degrees Celsius and 70 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
GS1	04250903201172 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K063042

FDA Product Code

• MWJ: Electrocardiograph,Ambulatory(Without Analysis)

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-21

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