Ethox

GUDID 30817357020794

Ethox Infu-Surg, 500cc

HYGIA HEALTH SERVICES, INC.

Intravenous pressure infusor, manual, reusable

• Primary Device ID: 30817357020794
• NIH Device Record Key: 5e8f6403-7152-4344-abdd-c596142b5a94
• Commercial Distribution Discontinuation: 2019-07-31
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Ethox
• Version Model Number: 4005
• Company DUNS: 177939027
• Company Name: HYGIA HEALTH SERVICES, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	10817357020790 [Primary]
GS1	30817357020794 [Package]; Contains: 10817357020790; Package: Box [5 Units]; Discontinued: 2021-03-19; Not in Commercial Distribution

FDA Product Code

• KZD: Infusor, Pressure, For I.V. Bags

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2021-03-19
• Device Publish Date: 2016-09-24

On-Brand Devices [Ethox]

• 30817357021074: Ethox Infu-Surg, 1000cc
• 30817357020923: Ethox Infu-Surg with Hook, 1000cc
• 30817357020800: Ethox Infu-Surg with Hook, 500cc
• 30817357020794: Ethox Infu-Surg, 500cc