TENS AA

GUDID 06942808221024

TENS AA is a Transcutaneous Electrical Nerve Stimulator which is used to provide symptomatic pain relief for chronic, acute or post operative pain.

EasyMed Instruments Co., Ltd.

Analgesic transcutaneous electrical nerve stimulation system

• Primary Device ID: 06942808221024
• NIH Device Record Key: 8841ef65-8b3d-4b22-ab3f-ad88e87f6231
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: TENS AA
• Version Model Number: TENS AA
• Company DUNS: 526951168
• Company Name: EasyMed Instruments Co., Ltd.
• 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: false
• Manufacturing Date: false
• 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
GS1	06942808221024 [Primary]

FDA Product Code

• GZJ: Stimulator, Nerve, Transcutaneous, For Pain Relief

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: 2019-10-23
• Device Publish Date: 2016-12-31

Devices Manufactured by EasyMed Instruments Co., Ltd.

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