LiteTouch

GUDID 00732671071323

MediCore's LiteTouch Brand Luer Lock Hypodermic Syringe w/Needle

AMITY HOLDINGS, LLC

Hypodermic needle, single-use

• Primary Device ID: 00732671071323
• NIH Device Record Key: 0291bde1-6d9e-4a9b-aefd-7b6dd0035605
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LiteTouch
• Version Model Number: 713LW
• Company DUNS: 016069284
• Company Name: AMITY HOLDINGS, 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: true

Customer Support Contacts

• Phone: 800 327 8894
• Email: wconety@medicore.com
• Phone: 800 327 8894
• Email: wconety@medicore.com

Device Dimensions

• Total Volume: 3 Milliliter
• Total Volume: 3 Milliliter
• Total Volume: 3 Milliliter
• Total Volume: 3 Milliliter
• Total Volume: 3 Milliliter
• Total Volume: 3 Milliliter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00732671071323 [Primary]
GS1	10732671171327 [Package]; Package: Chipboard carton [100 Units]
GS1	20732671271321 [Package]; Contains: 10732671171327; Package: Corrogate Carton [12 Units]

FDA Product Code

• FMI: Needle, Hypodermic, Single Lumen

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 9
• Public Version Date: 2019-10-23
• Device Publish Date: 2016-09-22

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