Female Luer Lock Cap 75309

GUDID 00853832007118

The Female Luer Lock Cap is for use on medical devices such as IV sets to cover female Luer fittings to reduce the risk of touch contamination and medication leakage.

MEDSAFETY SOLUTIONS LLC

Basic intravenous administration set, noninvasive

• Primary Device ID: 00853832007118
• NIH Device Record Key: 23a18f15-9261-40b6-8f1a-1687a0435fbd
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Female Luer Lock Cap
• Version Model Number: 75309
• Catalog Number: 75309
• Company DUNS: 080521478
• Company Name: MEDSAFETY SOLUTIONS 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

Customer Support Contacts

• Phone: 1-720-500-2500
• Email: info@medsafetysolutions.com
• Phone: 1-720-500-2500
• Email: info@medsafetysolutions.com
• Phone: 1-720-500-2500
• Email: info@medsafetysolutions.com
• Phone: 1-720-500-2500
• Email: info@medsafetysolutions.com
• Phone: 1-720-500-2500
• Email: info@medsafetysolutions.com
• Phone: 1-720-500-2500
• Email: info@medsafetysolutions.com
• Phone: 1-720-500-2500
• Email: info@medsafetysolutions.com
• Phone: 1-720-500-2500
• Email: info@medsafetysolutions.com
• Phone: 1-720-500-2500
• Email: info@medsafetysolutions.com
• Phone: 1-720-500-2500
• Email: info@medsafetysolutions.com
• Phone: 1-720-500-2500
• Email: info@medsafetysolutions.com
• Phone: 1-720-500-2500
• Email: info@medsafetysolutions.com
• Phone: 1-720-500-2500
• Email: info@medsafetysolutions.com
• Phone: 1-720-500-2500
• Email: info@medsafetysolutions.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00853832007118 [Primary]

FDA Product Code

• FPA: Set, Administration, Intravascular

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: 2021-04-07
• Device Publish Date: 2020-11-04

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