NAMIRSA

GUDID 06971712724680

Hong Qiangxing (Shen Zhen) Electronics Limited

Analgesic transcutaneous electrical nerve stimulation system

• Primary Device ID: 06971712724680
• NIH Device Record Key: 7bb4dbb3-c969-43b0-b4ca-eee5da96664d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: NAMIRSA
• Version Model Number: SM9033
• Company DUNS: 421286946
• Company Name: Hong Qiangxing (Shen Zhen) Electronics Limited
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• Human Cell/Tissue Product: false
• Device Kit: true
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• 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	06971712724680 [Primary]
GS1	16971712724687 [Package]; Package: [30 Units]; Discontinued: 2025-07-30; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K220283

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: 3
• Public Version Date: 2025-07-17
• Device Publish Date: 2023-02-15

On-Brand Devices [NAMIRSA]

• 06971712720712: ZX-603
• 06971712724680: SM9033