ClearView Total Uterine Manipulator

GUDID 00814247020499

ClearView Total Uterine Manipulator, regular tip (7cm)

CLINICAL INNOVATIONS, LLC

Colpotomy tube Colpotomy tube

• Primary Device ID: 00814247020499
• NIH Device Record Key: 6dd338a8-8a86-4e4e-89b9-5b293397a8c2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ClearView Total Uterine Manipulator
• Version Model Number: UM750
• Company DUNS: 809524291
• Company Name: CLINICAL INNOVATIONS, 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: true
• 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	00814247020499 [Primary]
GS1	10814247020496 [Package]; Package: [5 Units]; In Commercial Distribution
GS1	20814247020493 [Package]; Contains: 10814247020496; Package: [4 Units]; In Commercial Distribution

FDA Product Code

• LKF: Cannula, Manipulator/Injector, Uterine

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-09-01

On-Brand Devices [ClearView Total Uterine Manipulator]

• 20814247020615: ClearView Total Uterine Manipulator, 9cm tip
• 00814247020499: ClearView Total Uterine Manipulator, regular tip (7cm)