Ecogel 300

GUDID 00628055650539

5 Liter cubetainer

Eco-Med Pharmaceutical Inc

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• Primary Device ID: 00628055650539
• NIH Device Record Key: 7e9c35b1-836b-429a-aaf2-2208e39d84c6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Ecogel 300
• Version Model Number: 50TS
• Company DUNS: 249183435
• Company Name: Eco-Med Pharmaceutical Inc
• 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: false
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00628055650539 [Primary]
GS1	00628055650690 [Package]; Package: Case [4 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K962681

FDA Product Code

• GYB: Media, Electroconductive

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: 2020-01-15
• Device Publish Date: 2016-08-23

On-Brand Devices [Ecogel 300]

• 00628055650546: Single 5 Liter
• 00628055650539: 5 Liter cubetainer
• 00628055650522: 24x250ml case
• 00628055650515: 250ml bottle