BTL-299-6

GUDID B108299AP26ENUS011000

BTL INDUSTRIES LIMITED

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• Primary Device ID: B108299AP26ENUS011000
• NIH Device Record Key: 4d2a97a6-7275-4c20-a76b-ea9d14bcf99b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BTL-299-6
• Version Model Number: BTL-299-6
• Company DUNS: 733532951
• Company Name: BTL INDUSTRIES LIMITED
• 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: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	B108299AP26ENUS011000 [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: 2018-02-08

On-Brand Devices [BTL-299-6]

• B108299AP26ENUS011020: BTL-299-6
• B108299AP26ENUS011010: BTL-299-6
• B108299AP26ENUS011000: BTL-299-6
• B108299AP26ENUS011030: BTL-299-6