GUDID 06970341670870

diameter 50mm

GMDASZ manufacturing Co., Ltd.

Transcutaneous electrical stimulation electrode, single-use

• Primary Device ID: 06970341670870
• NIH Device Record Key: f4b2df8b-bdea-4c3e-a2bb-d67c5d5fdbf5
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: SBM1AC002
• Company DUNS: 529401134
• Company Name: GMDASZ manufacturing 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: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	06970341670870 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K160138

FDA Product Code

• GXY: Electrode, Cutaneous

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-05-07
• Device Publish Date: 2024-04-29

Devices Manufactured by GMDASZ manufacturing Co., Ltd.

• 06970341670542 - NA: 2026-01-02
• 06970341670740 - NA: 2026-01-02
• 06970341670764 - NA: 2026-01-02
• 06970341670771 - NA: 2026-01-02
• 06970341670818 - NA: 2026-01-02
• 06970341670825 - NA: 2026-01-02
• 06970341674014 - NA: 2026-01-02
• 06970341674069 - NA: 2026-01-02