Mediplus

GUDID 15055140702125

Double lumen cystometry catheter, 10fr

MEDIPLUS LTD

Urodynamic measurement system

• Primary Device ID: 15055140702125
• NIH Device Record Key: 3dde46a9-3195-4342-92b1-deb1259e9d58
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Mediplus
• Version Model Number: 5712
• Company DUNS: 228480810
• Company Name: MEDIPLUS LTD
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +4401494551200
• Email: help@mediplus.co.uk

Device Dimensions

• Catheter Gauge: 10 French
• Length: 65 Centimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	05055140702128 [Primary]
GS1	15055140702125 [Package]; Contains: 05055140702128; Package: [10 Units]; In Commercial Distribution

FDA Product Code

• KGZ: ACCESSORIES, CATHETER

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: 2016-09-16

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