DXTender DXT-L09

GUDID H671DXTL092

Angled Electrode Extender, 9cm Length

UTAH MEDICAL PRODUCTS, INC.

Open-surgery electrosurgical electrode, monopolar, single-use

• Primary Device ID: H671DXTL092
• NIH Device Record Key: 5712dabf-2fb4-4192-abac-a1e82c1a770e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DXTender
• Version Model Number: Large Electrode Extender
• Catalog Number: DXT-L09
• Company DUNS: 094651270
• Company Name: UTAH MEDICAL PRODUCTS, 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: 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

Customer Support Contacts

• Phone: 800-533-4984
• Email: customer@utahmed.com

Device Dimensions

• Length: 9 Centimeter

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	H671DXTL090 [Primary]
HIBCC	H671DXTL091 [Package]; Contains: H671DXTL090; Package: [10 Units]; In Commercial Distribution
HIBCC	H671DXTL092 [Package]; Contains: H671DXTL091; Package: [10 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K905263

FDA Product Code

• GEI: Electrosurgical, Cutting & Coagulation & Accessories

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2019-12-18
• Device Publish Date: 2016-09-23

On-Brand Devices [DXTender]

• H671DXTS062: Angled Electrode Extender, 6cm Length
• H671DXTL092: Angled Electrode Extender, 9cm Length