BEMER Therapy Systems 420200

GUDID 07640161461048

Bemer Int. AG

Hand-held deep-tissue electromagnetic stimulator

• Primary Device ID: 07640161461048
• NIH Device Record Key: 6dbf84ab-0a9e-4dd4-8b38-b6095e200ea7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BEMER Therapy Systems
• Version Model Number: B.BOX Professional
• Catalog Number: 420200
• Company DUNS: 448002860
• Company Name: Bemer Int. AG
• 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: false
• Serial Number: true
• Manufacturing Date: false
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	07640161461024 [Package]; Contains: 07640161462021; Package: [1 Units]; In Commercial Distribution
GS1	07640161461048 [Package]; Contains: 07640161462021; Package: [1 Units]; In Commercial Distribution
GS1	07640161462021 [Primary]

FDA Product Code

• NGX: Stimulator, Muscle, Powered, For Muscle Conditioning

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2017-05-03

On-Brand Devices [BEMER Therapy Systems]

• 07640161461048: B.BOX Professional
• 07640161461017: B.BOX Classic
• 07640161461055: Professional