EndoCurette CUR-120

GUDID H671CUR1201

Endometrial Suction Curette with Syringe

UTAH MEDICAL PRODUCTS, INC.

Endometrial biopsy curette

• Primary Device ID: H671CUR1201
• NIH Device Record Key: 6d360084-eda5-4d97-a254-f1731e086503
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: EndoCurette
• Version Model Number: Clear
• Catalog Number: CUR-120
• 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

• Outer Diameter: 3.1 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	H671CUR1200 [Primary]
HIBCC	H671CUR1201 [Package]; Contains: H671CUR1200; Package: Box [20 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K000974

FDA Product Code

• HHK: Curette, Suction, Endometrial (And 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: 4
• Public Version Date: 2019-12-18
• Device Publish Date: 2016-09-23

On-Brand Devices [EndoCurette]

• H671CUR1201: Endometrial Suction Curette with Syringe
• H671CUR1001: Endometrial Suction Curette