Oxiline

GUDID 06971712722266

Hong Qiangxing (Shen Zhen) Electronics Limited

Physical therapy transcutaneous neuromuscular electrical stimulation system

• Primary Device ID: 06971712722266
• NIH Device Record Key: b361d910-a50b-42ff-8b00-886df7afe9d4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Oxiline
• Version Model Number: OXILINE TENS PRO
• Company DUNS: 421286946
• Company Name: Hong Qiangxing (Shen Zhen) Electronics Limited
• Device Count: 1
• DM Exempt: true
• 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: true
• 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	06971712722266 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K201354

FDA Product Code

• NUH: Stimulator, Nerve, Transcutaneous, Over-The-Counter

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: 2024-11-11
• Device Publish Date: 2022-08-25

On-Brand Devices [Oxiline]

• 06971712722259: TENS
• 06971712722266: OXILINE TENS PRO