SNAPTRACE 1921-100

GUDID 20653405039140

SNAPTRACE II RESTING SNAP

Conmed Corporation

Electrocardiographic electrode, single-use

• Primary Device ID: 20653405039140
• NIH Device Record Key: d0ff3e0c-469c-49ad-b56c-c19eecdbd60a
• Commercial Distribution Discontinuation: 2023-05-12
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: SNAPTRACE
• Version Model Number: 1921-100
• Catalog Number: 1921-100
• Company DUNS: 071595540
• Company Name: Conmed Corporation
• Device Count: 1000
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Safe
• 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: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM

Operating and Storage Conditions

• Handling Environment Humidity: Between -4 Percent (%) Relative Humidity and 131 Percent (%) Relative Humidity
• Handling Environment Humidity: Between -4 Percent (%) Relative Humidity and 131 Percent (%) Relative Humidity
• Handling Environment Humidity: Between -4 Percent (%) Relative Humidity and 131 Percent (%) Relative Humidity
• Handling Environment Humidity: Between -4 Percent (%) Relative Humidity and 131 Percent (%) Relative Humidity
• Handling Environment Humidity: Between -4 Percent (%) Relative Humidity and 131 Percent (%) Relative Humidity
• Handling Environment Humidity: Between -4 Percent (%) Relative Humidity and 131 Percent (%) Relative Humidity
• Handling Environment Humidity: Between -4 Percent (%) Relative Humidity and 131 Percent (%) Relative Humidity
• Handling Environment Humidity: Between -4 Percent (%) Relative Humidity and 131 Percent (%) Relative Humidity
• Handling Environment Humidity: Between -4 Percent (%) Relative Humidity and 131 Percent (%) Relative Humidity
• Handling Environment Humidity: Between -4 Percent (%) Relative Humidity and 131 Percent (%) Relative Humidity
• Handling Environment Humidity: Between -4 Percent (%) Relative Humidity and 131 Percent (%) Relative Humidity
• Handling Environment Humidity: Between -4 Percent (%) Relative Humidity and 131 Percent (%) Relative Humidity
• Handling Environment Humidity: Between -4 Percent (%) Relative Humidity and 131 Percent (%) Relative Humidity
• Handling Environment Humidity: Between -4 Percent (%) Relative Humidity and 131 Percent (%) Relative Humidity
• Handling Environment Humidity: Between -4 Percent (%) Relative Humidity and 131 Percent (%) Relative Humidity
• Handling Environment Humidity: Between -4 Percent (%) Relative Humidity and 131 Percent (%) Relative Humidity

Device Identifiers

Device Issuing Agency	Device ID
GS1	00653405039146 [Unit of Use]
GS1	10653405039143 [Primary]
GS1	20653405039140 [Package]; Contains: 10653405039143; Package: BOX [1000 Units]; Discontinued: 2023-05-12; Not in Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K910494

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: 4
• Public Version Date: 2023-05-15
• Device Publish Date: 2016-09-24

On-Brand Devices [SNAPTRACE]

• 20653405004599: SNAPTRACE 50 FM, WTGEL
• 20653405039140: SNAPTRACE II RESTING SNAP