Rebound refill kit SBTR200

GUDID 00857771003026

ea

BIOMEDICAL LIFE SYSTEMS, INC.

Transcutaneous electrical stimulation electrode Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use

• Primary Device ID: 00857771003026
• NIH Device Record Key: 96465745-5138-4489-80f3-da0eac9d93d6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Rebound refill kit
• Version Model Number: SBTR200
• Catalog Number: SBTR200
• Company DUNS: 116956807
• Company Name: BIOMEDICAL LIFE SYSTEMS, INC.
• 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: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 7607575600
• Email: information@bmls.com
• Phone: 7607575600
• Email: information@bmls.com
• Phone: 7607575600
• Email: information@bmls.com
• Phone: 7607575600
• Email: information@bmls.com
• Phone: 7607575600
• Email: information@bmls.com
• Phone: 7607575600
• Email: information@bmls.com
• Phone: 7607575600
• Email: information@bmls.com
• Phone: 7607575600
• Email: information@bmls.com
• Phone: 7607575600
• Email: information@bmls.com
• Phone: 7607575600
• Email: information@bmls.com
• Phone: 7607575600
• Email: information@bmls.com
• Phone: 7607575600
• Email: information@bmls.com
• Phone: 7607575600
• Email: information@bmls.com
• Phone: 7607575600
• Email: information@bmls.com
• Phone: 7607575600
• Email: information@bmls.com
• Phone: 7607575600
• Email: information@bmls.com
• Phone: 7607575600
• Email: information@bmls.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00857771003026 [Primary]

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: 3
• Public Version Date: 2019-06-28
• Device Publish Date: 2016-09-23

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