EZ Regular

GUDID 38809289430217

EZ Regular N410

Meinntech Co., Ltd.

Intravenous administration set Intravenous administration set Basic intravenous administration set, noninvasive Basic intravenous administration set, noninvasive Basic intravenous administration set, noninvasive Basic intravenous administration set, noninvasive Basic intravenous administration set, noninvasive Basic intravenous administration set, noninvasive Basic intravenous administration set, noninvasive Basic intravenous administration set, noninvasive Basic intravenous administration set, noninvasive Basic intravenous administration set, noninvasive Basic intravenous administration set, noninvasive Basic intravenous administration set, noninvasive Basic intravenous administration set, noninvasive Basic intravenous administration set, noninvasive

• Primary Device ID: 38809289430217
• NIH Device Record Key: d1d1d6ce-68fa-47ed-bb26-1cbe9a98b38c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: EZ Regular
• Version Model Number: N410
• Company DUNS: 688438097
• Company Name: Meinntech Co., Ltd.
• 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: 800-969-6331
• Email: CS@progressivemedinc.com
• Phone: 800-969-6331
• Email: CS@progressivemedinc.com
• Phone: 800-969-6331
• Email: CS@progressivemedinc.com
• Phone: 800-969-6331
• Email: CS@progressivemedinc.com
• Phone: 800-969-6331
• Email: CS@progressivemedinc.com
• Phone: 800-969-6331
• Email: CS@progressivemedinc.com
• Phone: 800-969-6331
• Email: CS@progressivemedinc.com
• Phone: 800-969-6331
• Email: CS@progressivemedinc.com
• Phone: 800-969-6331
• Email: CS@progressivemedinc.com
• Phone: 800-969-6331
• Email: CS@progressivemedinc.com
• Phone: 800-969-6331
• Email: CS@progressivemedinc.com
• Phone: 800-969-6331
• Email: CS@progressivemedinc.com
• Phone: 800-969-6331
• Email: CS@progressivemedinc.com
• Phone: 800-969-6331
• Email: CS@progressivemedinc.com
• Phone: 800-969-6331
• Email: CS@progressivemedinc.com
• Phone: 800-969-6331
• Email: CS@progressivemedinc.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	18809289430190 [Primary]
GS1	28809289430203 [Package]; Contains: 18809289430190; Package: [25 Units]; In Commercial Distribution
GS1	38809289430217 [Package]; Contains: 28809289430203; Package: [10 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K080303

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: 4
• Public Version Date: 2019-12-11
• Device Publish Date: 2016-11-29

On-Brand Devices [EZ Regular]

• 38809289430217: EZ Regular N410
• 38809289430163: EZ Regular N112
• 38809289430101: EZ Regular N110