EZ Regular

GUDID 38809289430163

EZ Regular N112

Meinntech Co., Ltd.

Intravenous administration set

• Primary Device ID: 38809289430163
• NIH Device Record Key: 68e80751-9cae-4b13-95d6-3958df48f0c1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: EZ Regular
• Version Model Number: N112
• 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	18809289430145 [Primary]
GS1	28809289430159 [Package]; Contains: 18809289430145; Package: [25 Units]; In Commercial Distribution
GS1	38809289430163 [Package]; Contains: 28809289430159; 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