ActiPatch 090-4

GUDID 00851329005470

ActiPatch Back Pain Relief Therapy 100 pack

Bioelectronics Corporation

Hand-held deep-tissue electromagnetic stimulator Hand-held deep-tissue electromagnetic stimulator Hand-held deep-tissue electromagnetic stimulator Hand-held deep-tissue electromagnetic stimulator Hand-held deep-tissue electromagnetic stimulator Hand-held deep-tissue electromagnetic stimulator Hand-held deep-tissue electromagnetic stimulator Hand-held deep-tissue electromagnetic stimulator Hand-held deep-tissue electromagnetic stimulator Hand-held deep-tissue electromagnetic stimulator Hand-held deep-tissue electromagnetic stimulator Hand-held deep-tissue electromagnetic stimulator Hand-held deep-tissue electromagnetic stimulator Hand-held deep-tissue electromagnetic stimulator Hand-held deep-tissue electromagnetic stimulator Hand-held deep-tissue electromagnetic stimulator

• Primary Device ID: 00851329005470
• NIH Device Record Key: 4df545c0-a903-46b7-9a53-ee35e1f6c3e2
• Commercial Distribution Discontinuation: 2021-06-09
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: ActiPatch
• Version Model Number: 088
• Catalog Number: 090-4
• 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: false
• Device Combination Product: false
• Single Use: true
• 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: false
• RX Perscription: false
• OTC Over-The-Counter: true

Customer Support Contacts

• Phone: 3018744890
• Email: skoneru@bielcorp.com
• Phone: 3018744890
• Email: skoneru@bielcorp.com
• Phone: 3018744890
• Email: skoneru@bielcorp.com
• Phone: 3018744890
• Email: skoneru@bielcorp.com
• Phone: 3018744890
• Email: skoneru@bielcorp.com
• Phone: 3018744890
• Email: skoneru@bielcorp.com
• Phone: 3018744890
• Email: skoneru@bielcorp.com
• Phone: 3018744890
• Email: skoneru@bielcorp.com
• Phone: 3018744890
• Email: skoneru@bielcorp.com
• Phone: 3018744890
• Email: skoneru@bielcorp.com
• Phone: 3018744890
• Email: skoneru@bielcorp.com
• Phone: 3018744890
• Email: skoneru@bielcorp.com
• Phone: 3018744890
• Email: skoneru@bielcorp.com
• Phone: 3018744890
• Email: skoneru@bielcorp.com
• Phone: 3018744890
• Email: skoneru@bielcorp.com
• Phone: 3018744890
• Email: skoneru@bielcorp.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00851329005470 [Primary]

FDA Product Code

• PQY: Nonthermal Shortwave Therapy Device Indicated For Over The Counter Use For The Treatment Of Pain

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-06-17
• Device Publish Date: 2021-06-09

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