ActiPatch 090-4B

GUDID 00851329005050

Back Pain Advanced long -Lasting Relief

Bioelectronics Corporation

Hand-held deep-tissue electromagnetic stimulator

• Primary Device ID: 00851329005050
• NIH Device Record Key: 1cd4255d-7aa2-4fb7-99c3-44dafdf530fb
• Commercial Distribution Discontinuation: 2019-09-10
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: ActiPatch
• Version Model Number: 088
• Catalog Number: 090-4B
• Company DUNS: 101591571
• Company Name: Bioelectronics Corporation
• 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: true
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: true
• Manufacturing Date: true
• 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: 3018744890
• Email: ljarman@bielcorp.com
• Phone: 3018744890
• Email: ljarman@bielcorp.com
• Phone: 3018744890
• Email: ljarman@bielcorp.com
• Phone: 3018744890
• Email: ljarman@bielcorp.com
• Phone: 3018744890
• Email: ljarman@bielcorp.com
• Phone: 3018744890
• Email: ljarman@bielcorp.com
• Phone: 3018744890
• Email: ljarman@bielcorp.com
• Phone: 3018744890
• Email: ljarman@bielcorp.com
• Phone: 3018744890
• Email: ljarman@bielcorp.com
• Phone: 3018744890
• Email: ljarman@bielcorp.com
• Phone: 3018744890
• Email: ljarman@bielcorp.com
• Phone: 3018744890
• Email: ljarman@bielcorp.com
• Phone: 3018744890
• Email: ljarman@bielcorp.com
• Phone: 3018744890
• Email: brice@bielcorp.com
• Phone: 3018744890
• Email: brice@bielcorp.com
• Phone: 3018744890
• Email: brice@bielcorp.com
• Phone: 3018744890
• Email: brice@bielcorp.com
• Phone: 3018744890
• Email: brice@bielcorp.com
• Phone: 3018744890
• Email: brice@bielcorp.com
• Phone: 3018744890
• Email: brice@bielcorp.com
• Phone: 3018744890
• Email: brice@bielcorp.com
• Phone: 3018744890
• Email: brice@bielcorp.com
• Phone: 3018744890
• Email: brice@bielcorp.com
• Phone: 3018744890
• Email: brice@bielcorp.com
• Phone: 3018744890
• Email: brice@bielcorp.com

Device Dimensions

• Outer Diameter: 15 Inch
• Outer Diameter: 15 Inch
• Outer Diameter: 15 Inch
• Outer Diameter: 15 Inch
• Outer Diameter: 15 Inch
• Outer Diameter: 15 Inch
• Outer Diameter: 15 Inch
• Outer Diameter: 15 Inch
• Outer Diameter: 15 Inch
• Outer Diameter: 15 Inch
• Outer Diameter: 15 Inch
• Outer Diameter: 15 Inch
• Outer Diameter: 15 Inch

Operating and Storage Conditions

• Handling Environment Temperature: Between 55 Degrees Fahrenheit and 110 Degrees Fahrenheit
• Handling Environment Temperature: Between 55 Degrees Fahrenheit and 110 Degrees Fahrenheit
• Handling Environment Temperature: Between 55 Degrees Fahrenheit and 110 Degrees Fahrenheit
• Handling Environment Temperature: Between 55 Degrees Fahrenheit and 110 Degrees Fahrenheit
• Handling Environment Temperature: Between 55 Degrees Fahrenheit and 110 Degrees Fahrenheit
• Handling Environment Temperature: Between 55 Degrees Fahrenheit and 110 Degrees Fahrenheit
• Handling Environment Temperature: Between 55 Degrees Fahrenheit and 110 Degrees Fahrenheit
• Handling Environment Temperature: Between 55 Degrees Fahrenheit and 110 Degrees Fahrenheit
• Handling Environment Temperature: Between 55 Degrees Fahrenheit and 110 Degrees Fahrenheit
• Handling Environment Temperature: Between 55 Degrees Fahrenheit and 110 Degrees Fahrenheit
• Handling Environment Temperature: Between 55 Degrees Fahrenheit and 110 Degrees Fahrenheit
• Handling Environment Temperature: Between 55 Degrees Fahrenheit and 110 Degrees Fahrenheit
• Handling Environment Temperature: Between 55 Degrees Fahrenheit and 110 Degrees Fahrenheit

Device Identifiers

Device Issuing Agency	Device ID
GS1	00851329005050 [Primary]

FDA Product Code

• ILX: Diathermy, Shortwave, For Use Other Than Applying Therapeutic Deep Heat

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: 2019-09-10
• Device Publish Date: 2015-07-22

On-Brand Devices [ActiPatch]

• 00851329005050: Back Pain Advanced long -Lasting Relief
• 00851329005340: Back, Knee, Muscle & Joint Advanced Long-Lasting Relief.
• 00851329005203: Back , Knee, Muscle and Joint 7 day trial
• 00851329005159: Back Pain Advanced Long-Lasting Relief
• 00851329005012: Knee Pain Advanced Long-Lasting Relief
• 80851329005155: ActiPatch Back Pain Therapy Kit 5 pack
• 00851329005494: ActiPatch Muscle and Joint Relief Therapy 100 pack
• 00851329005487: ActiPatch Knee Pain Relief Therapy 100 pack
• 00851329005470: ActiPatch Back Pain Relief Therapy 100 pack
• 00851329005258: ActiPatch Muscle and Joint Pain Therapy Kit 5 pack
• 00851329005241: ActiPatch Knee Pain Therapy Device 5 pack