AtoN Keywest Headlight with 7' Fiber Optic Cable

GUDID 00851610007176

Light, Surgical, Endoscopic, Accessory

LONG ISLAND TECH

Endoscopic light source, line-powered Endoscopic light source unit, line-powered Endoscopic light source unit, line-powered Endoscopic light source unit, line-powered Endoscopic light source unit, line-powered Endoscopic light source unit, line-powered Endoscopic light source unit, line-powered Endoscopic light source unit, line-powered Endoscopic light source unit, line-powered Endoscopic light source unit, line-powered Endoscopic light source unit, line-powered Endoscopic light source unit, line-powered Endoscopic light source unit, line-powered Endoscopic light source unit, line-powered Endoscopic light source unit, line-powered

• Primary Device ID: 00851610007176
• NIH Device Record Key: 8f308eef-f47c-453f-988a-d8bf0a6cc12b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AtoN Keywest Headlight with 7' Fiber Optic Cable
• Version Model Number: P003262
• Company DUNS: 030256600
• Company Name: LONG ISLAND TECH
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00851610007176 [Primary]

FDA Product Code

• FSW: Light, Surgical, Endoscopic

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: 2019-02-21
• Device Publish Date: 2016-09-02