Ecomed Angiographic 128-I60195

GUDID 00855009006030

60" Coiled Extension Tubing, high pressure

ECOMED SOLUTIONS, LLC

Radiographic procedure tubing

• Primary Device ID: 00855009006030
• NIH Device Record Key: 743b6935-97a6-41e3-bc60-86bac125fd60
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Ecomed Angiographic
• Version Model Number: 128-I60195
• Catalog Number: 128-I60195
• Company DUNS: 079814353
• Company Name: ECOMED SOLUTIONS, LLC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Safe
• 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: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(866)817-7114
• Email: onestop@ecomed-solutions.com

Device Dimensions

• Pressure: 300 Pound per Square Inch
• Pressure: 300 Pound per Square Inch

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry

Device Identifiers

Device Issuing Agency	Device ID
GS1	00855009006030 [Primary]
GS1	10855009006037 [Package]; Package: Case [50 Units]; In Commercial Distribution

FDA Product Code

• DXT: Injector And Syringe, Angiographic

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2017-09-21

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