NeoLead 989803183131

GUDID 20884838035175

Philips Medical Systems

Electrocardiographic electrode, single-use

• Primary Device ID: 20884838035175
• NIH Device Record Key: ff2721b4-91e5-4dac-93d3-384720bb7c2b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: NeoLead
• Version Model Number: 989803183131
• Catalog Number: 989803183131
• Company DUNS: 078628040
• Company Name: Philips Medical Systems
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Customer Support Contacts

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Device Identifiers

Device Issuing Agency	Device ID
GS1	20884838035175 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K011564

FDA Product Code

• DRX: Electrode, electrocardiograph

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: 2017-02-16

On-Brand Devices [NeoLead]

• 20884838035182: 989803183141
• 20884838035175: 989803183131
• 20884838035168: 989803183121
• 20884838035151: 989803183111
• 20884838035144: 989803183101
• 20884838035137: 989803183091
• 20884838035106: 989803183081