VEINOPLUS PACK

GUDID 03701084900008

AD REM TECHNOLOGY

Transcutaneous electrical stimulation electrode, single-use

• Primary Device ID: 03701084900008
• NIH Device Record Key: 15a67fad-22f3-4256-9a52-ef842130eeb5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VEINOPLUS PACK
• Version Model Number: 8x13 OVAL
• Company DUNS: 273234679
• Company Name: AD REM TECHNOLOGY
• 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: 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: true

Customer Support Contacts

• Phone: +33(0)142600022
• Email: info@veinoplus.com
• Phone: +33(0)142600022
• Email: info@veinoplus.com
• Phone: +33(0)142600022
• Email: info@veinoplus.com
• Phone: +33(0)142600022
• Email: info@veinoplus.com
• Phone: +33(0)142600022
• Email: info@veinoplus.com
• Phone: +33(0)142600022
• Email: info@veinoplus.com
• Phone: +33(0)142600022
• Email: info@veinoplus.com
• Phone: +33(0)142600022
• Email: info@veinoplus.com
• Phone: +33(0)142600022
• Email: info@veinoplus.com
• Phone: +33(0)142600022
• Email: info@veinoplus.com
• Phone: +33(0)142600022
• Email: info@veinoplus.com
• Phone: +33(0)142600022
• Email: info@veinoplus.com
• Phone: +33(0)142600022
• Email: info@veinoplus.com
• Phone: +33(0)142600022
• Email: info@veinoplus.com
• Phone: +33(0)142600022
• Email: info@veinoplus.com
• Phone: +33(0)142600022
• Email: info@veinoplus.com

Operating and Storage Conditions

• Storage Environment Temperature: Between 41 Degrees Fahrenheit and 80.6 Degrees Fahrenheit
• Storage Environment Temperature: Between 41 Degrees Fahrenheit and 80.6 Degrees Fahrenheit
• Storage Environment Temperature: Between 41 Degrees Fahrenheit and 80.6 Degrees Fahrenheit
• Storage Environment Temperature: Between 41 Degrees Fahrenheit and 80.6 Degrees Fahrenheit
• Storage Environment Temperature: Between 41 Degrees Fahrenheit and 80.6 Degrees Fahrenheit
• Storage Environment Temperature: Between 41 Degrees Fahrenheit and 80.6 Degrees Fahrenheit
• Storage Environment Temperature: Between 41 Degrees Fahrenheit and 80.6 Degrees Fahrenheit
• Storage Environment Temperature: Between 41 Degrees Fahrenheit and 80.6 Degrees Fahrenheit
• Storage Environment Temperature: Between 41 Degrees Fahrenheit and 80.6 Degrees Fahrenheit
• Storage Environment Temperature: Between 41 Degrees Fahrenheit and 80.6 Degrees Fahrenheit
• Storage Environment Temperature: Between 41 Degrees Fahrenheit and 80.6 Degrees Fahrenheit
• Storage Environment Temperature: Between 41 Degrees Fahrenheit and 80.6 Degrees Fahrenheit
• Storage Environment Temperature: Between 41 Degrees Fahrenheit and 80.6 Degrees Fahrenheit
• Storage Environment Temperature: Between 41 Degrees Fahrenheit and 80.6 Degrees Fahrenheit
• Storage Environment Temperature: Between 41 Degrees Fahrenheit and 80.6 Degrees Fahrenheit
• Storage Environment Temperature: Between 41 Degrees Fahrenheit and 80.6 Degrees Fahrenheit

Device Identifiers

Device Issuing Agency	Device ID
GS1	03701084900008 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K141919

FDA Product Code

• GXY: Electrode, Cutaneous

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: 2021-02-19
• Device Publish Date: 2016-09-19

Devices Manufactured by AD REM TECHNOLOGY

• 03701084900008 - VEINOPLUS PACK: 2021-02-19
• 03701084900008 - VEINOPLUS PACK: 2021-02-19
• 03701084900015 - VEINOPLUS: 2019-10-23
• 03701084900022 - VEINOPLUS DVT: 2019-10-23
• 03701084900039 - VEINOPLUS SPORT: 2019-10-23