E Surgical RB4050-01

GUDID 00850053927041

4.0MM 50° ABLATOR

E Surgical, LLC

Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Endoscopic electrosurgical handpiece/electrode, bipolar, single-use

• Primary Device ID: 00850053927041
• NIH Device Record Key: 7e956db1-ed63-4a39-95f2-6adb9fabeeea
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: E Surgical
• Version Model Number: RB4050-01
• Catalog Number: RB4050-01
• Company DUNS: 093415510
• Company Name: E Surgical, LLC
• 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: 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850053927041 [Primary]

FDA Product Code

• GEI: Electrosurgical, Cutting & Coagulation & Accessories

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: 2024-06-03
• Device Publish Date: 2024-05-26

On-Brand Devices [E Surgical]

• 00850053927041: 4.0MM 50° ABLATOR
• 10850053927031: 4.0MM 50° ASPIRATING ABLATOR
• 10850053927024: 4.0MM 90° ABLATOR
• 00850053927010: 4.0MM 90° ASPIRATING ABLATOR