FMT

GUDID 08698870315816

Reusable ECG - EKG Cables and Leadwires

METKO MEDIKAL VE TIBBI CIHAZLAR DIS TICARET LIMITED SIRKETI

Electrocardiographic lead set, reusable

• Primary Device ID: 08698870315816
• NIH Device Record Key: 85d3ea7e-df00-48ba-b9f7-afeca8cc16e4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: FMT
• Version Model Number: E201-3060/GI
• Company DUNS: 566222169
• Company Name: METKO MEDIKAL VE TIBBI CIHAZLAR DIS TICARET LIMITED SIRKETI
• 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: true
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 415 802-4021
• Email: burcufirat@metkoltd.com
• Phone: 415 802-4021
• Email: burcufirat@metkoltd.com
• Phone: 415 802-4021
• Email: burcufirat@metkoltd.com
• Phone: 415 802-4021
• Email: burcufirat@metkoltd.com
• Phone: 415 802-4021
• Email: burcufirat@metkoltd.com
• Phone: 415 802-4021
• Email: burcufirat@metkoltd.com
• Phone: 415 802-4021
• Email: burcufirat@metkoltd.com
• Phone: 415 802-4021
• Email: burcufirat@metkoltd.com
• Phone: 415 802-4021
• Email: burcufirat@metkoltd.com
• Phone: 415 802-4021
• Email: burcufirat@metkoltd.com
• Phone: 415 802-4021
• Email: burcufirat@metkoltd.com
• Phone: 415 802-4021
• Email: burcufirat@metkoltd.com
• Phone: 415 802-4021
• Email: burcufirat@metkoltd.com
• Phone: 415 802-4021
• Email: burcufirat@metkoltd.com
• Phone: 415 802-4021
• Email: burcufirat@metkoltd.com
• Phone: 415 802-4021
• Email: burcufirat@metkoltd.com

Operating and Storage Conditions

• Storage Environment Temperature: Between 0 Degrees Celsius and 50 Degrees Celsius
• Storage Environment Temperature: Between 0 Degrees Celsius and 50 Degrees Celsius
• Storage Environment Temperature: Between 0 Degrees Celsius and 50 Degrees Celsius
• Storage Environment Temperature: Between 0 Degrees Celsius and 50 Degrees Celsius
• Storage Environment Temperature: Between 0 Degrees Celsius and 50 Degrees Celsius
• Storage Environment Temperature: Between 0 Degrees Celsius and 50 Degrees Celsius
• Storage Environment Temperature: Between 0 Degrees Celsius and 50 Degrees Celsius
• Storage Environment Temperature: Between 0 Degrees Celsius and 50 Degrees Celsius
• Storage Environment Temperature: Between 0 Degrees Celsius and 50 Degrees Celsius
• Storage Environment Temperature: Between 0 Degrees Celsius and 50 Degrees Celsius
• Storage Environment Temperature: Between 0 Degrees Celsius and 50 Degrees Celsius
• Storage Environment Temperature: Between 0 Degrees Celsius and 50 Degrees Celsius
• Storage Environment Temperature: Between 0 Degrees Celsius and 50 Degrees Celsius
• Storage Environment Temperature: Between 0 Degrees Celsius and 50 Degrees Celsius
• Storage Environment Temperature: Between 0 Degrees Celsius and 50 Degrees Celsius
• Storage Environment Temperature: Between 0 Degrees Celsius and 50 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
GS1	08698870315816 [Primary]

FDA Product Code

• IKD: Cable, Electrode

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: 2024-06-06
• Device Publish Date: 2020-05-22

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