STIMPOD NMS460

GUDID 00850070096003

ALGIAMED TECHNOLOGIES USA INC.

Analgesic transcutaneous electrical nerve stimulation system

• Primary Device ID: 00850070096003
• NIH Device Record Key: 62a015ae-491c-43f7-8bbb-4bd383513b17
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: STIMPOD NMS460
• Version Model Number: AL-46000
• Company DUNS: 134062881
• Company Name: ALGIAMED TECHNOLOGIES USA INC.
• 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: true
• 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850070096003 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K161091

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: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-05-14
• Device Publish Date: 2025-05-06

Devices Manufactured by ALGIAMED TECHNOLOGIES USA INC.

• 00850070096003 - STIMPOD NMS460: 2025-05-14
• 00850070096003 - STIMPOD NMS460: 2025-05-14
• 00850070096010 - STIMPOD NMS460 Kit: 2025-05-14
• 00850070096027 - Pulsed Radio Frequency Nerve Stimulation Cable: 2025-05-14