Nurokor

GUDID 00508556300136

Hong Qiangxing (Shen Zhen) Electronics Limited

Physical therapy transcutaneous neuromuscular electrical stimulation system

• Primary Device ID: 00508556300136
• NIH Device Record Key: e6dcd414-221c-4e99-8b47-b051748311ec
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Nurokor
• Version Model Number: Accessory
• Company DUNS: 421286946
• Company Name: Hong Qiangxing (Shen Zhen) Electronics Limited
• Device Count: 50
• 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: false
• 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	00508556300136 [Primary]
GS1	00868556300100 [Unit of Use]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K121719

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: 2018-11-06

On-Brand Devices [Nurokor]

• 00508556300136: Accessory
• 80001807361000: TENS
• 06971712720231: TENS
• 06971712720439: TENS
• 06971712720675: massage gloves
• 06971712720774: TENS
• 06971712725601: TENS
• 06971712727186: TENS