Scorpion

GUDID IDKWSF5125

NEUROVISION MEDICAL PRODUCTS, INC.

Nerve-locating system probe, single-use

• Primary Device ID: IDKWSF5125
• NIH Device Record Key: 1af9aec3-8bd0-4e19-80b3-ff6b5628b4a8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Scorpion
• Version Model Number: N/A
• Company DUNS: 182057401
• Company Name: NEUROVISION MEDICAL PRODUCTS, INC.
• Device Count: 5
• 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: true
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00810155860622 [Secondary]
HIBCC	B006IDKWSF5125 [Unit of Use]
HIBCC	B006IDKWSF51252 [Primary]
HIBCC	IDKWSF5125 [Package]; Contains: B006IDKWSF5125; Package: [5 Units]; In Commercial Distribution

FDA Product Code

• ETN: Stimulator, Nerve

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-09-11
• Device Publish Date: 2023-09-01

On-Brand Devices [Scorpion]

• B006T61075D0: N/A
• B006ICSI0: N/A
• B006IATF714BL0: N/A
• B006IATF714B0: N/A
• IDKMF512B5: N/A
• IDKATF714B5: N/A
• IDKWSF5125: N/A