Stimuplex® HNS 12 4892098

GUDID 04260166372083

Stimuplex® HNS 12 Nerv Stimulator with electrode cable / Electrode Cable Ordering-No. 4892070

Stockert GmbH

Nerve-locating system

• Primary Device ID: 04260166372083
• NIH Device Record Key: 2673d6f0-632b-4c02-9785-820620353ed8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Stimuplex® HNS 12
• Version Model Number: 4892098
• Catalog Number: 4892098
• Company DUNS: 327536314
• Company Name: Stockert GmbH
• 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: true
• 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: true
• OTC Over-The-Counter: false

Operating and Storage Conditions

• Storage Environment Temperature: Between 0 Degrees Celsius and 40 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
GS1	04260166372083 [Primary]

FDA Product Code

• BXN: Stimulator, Nerve, Battery-Powered

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: 2018-04-25
• Device Publish Date: 2017-05-04

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