Delasco Electricator 26000

GUDID 00609960000251

DESCRIPTION The Delasco Electricator is a non-sterile, reusable, electrosurgical generator. The Electricator is designed to generate high frequencies (radio frequency “RF”) of high voltage and low amperage current. The unit incorporates a ground-referenced monopolar and bipolar output which is used primarily in physician’s offices and treatment rooms to perform electrosurgical desiccation, fulguration, and coagulation procedures (described below). Patients with dermatological lesions such as cysts, polyps, and carbuncles can be treated with the Electricator with or without the use of anesthesia (depending on the site of the procedure and the patient tolerance level). INTENDED USE The Delasco Electricator is intended to be utilized for destroying skin lesions and to coagulate small bleeders by applying high frequency current. The unit is used primarily in the Physician’s office and in particular, those of Dermatologists and Plastic Surgeons.

DERMATOLOGIC LAB AND SUPPLY, INC.

Electrosurgical system generator

• Primary Device ID: 00609960000251
• NIH Device Record Key: 15442ab9-bb15-424c-9d74-623a461a80e8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Delasco Electricator
• Version Model Number: 26000
• Catalog Number: 26000
• Company DUNS: 021628771
• Company Name: DERMATOLOGIC LAB AND SUPPLY, 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: 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	00609960000251 [Primary]

FDA Product Code

• GEI: Electrosurgical, Cutting & Coagulation & Accessories

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: 2018-03-29
• Device Publish Date: 2016-05-19

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