WIEMSPRO

GUDID 08435393716450

MEDICAL CABLES SL

Physical therapy transcutaneous neuromuscular electrical stimulation system

• Primary Device ID: 08435393716450
• NIH Device Record Key: 2137ecb1-0065-4f94-8132-32bf984baf03
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: WIEMSPRO
• Version Model Number: WIEMSPRO
• Company DUNS: 463622207
• Company Name: MEDICAL CABLES SL
• 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: 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	08435393716450 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K181955

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: 2
• Public Version Date: 2019-10-23
• Device Publish Date: 2019-05-15