Coleman Luer Lock Cap COL-LLCAP

GUDID 10081317023484

Coleman Luer Lock Cap

MENTOR TEXAS L.P.

Syringe tip cap Luer-formatted protective cap Luer-formatted protective cap Luer-formatted protective cap Luer-formatted protective cap Luer-formatted protective cap Luer-formatted protective cap Luer-formatted protective cap Luer-formatted protective cap Luer-formatted protective cap Luer-formatted protective cap Luer-formatted protective cap Luer-formatted protective cap Luer-formatted protective cap Luer-formatted protective cap Luer-formatted protective cap

• Primary Device ID: 10081317023484
• NIH Device Record Key: 99ce393b-b73f-4ad7-afab-f005d962117c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Coleman Luer Lock Cap
• Version Model Number: COL-LLCAP
• Catalog Number: COL-LLCAP
• Company DUNS: 167450993
• Company Name: MENTOR TEXAS L.P.
• Device Count: 6
• 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: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)235-5731
• Email: xx@xx.xx
• Phone: +1(800)235-5731
• Email: xx@xx.xx
• Phone: +1(800)235-5731
• Email: xx@xx.xx
• Phone: +1(800)235-5731
• Email: xx@xx.xx
• Phone: +1(800)235-5731
• Email: xx@xx.xx
• Phone: +1(800)235-5731
• Email: xx@xx.xx
• Phone: +1(800)235-5731
• Email: xx@xx.xx
• Phone: +1(800)235-5731
• Email: xx@xx.xx
• Phone: +1(800)235-5731
• Email: xx@xx.xx
• Phone: +1(800)235-5731
• Email: xx@xx.xx
• Phone: +1(800)235-5731
• Email: xx@xx.xx
• Phone: +1(800)235-5731
• Email: xx@xx.xx
• Phone: +1(800)235-5731
• Email: xx@xx.xx
• Phone: +1(800)235-5731
• Email: xx@xx.xx
• Phone: +1(800)235-5731
• Email: xx@xx.xx
• Phone: +1(800)235-5731
• Email: xx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
GS1	00081317023487 [Primary]
GS1	10081317023484 [Package]; Contains: 00081317023487; Package: 25 Pouches/Box [25 Units]; In Commercial Distribution
GS1	20081317023481 [Unit of Use]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K981172

FDA Product Code

• MUU: System, suction, lipoplasty

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-14

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