Ecomed Angiographic 128-200301

GUDID 10855009006105

MR 60/60mL LF Dual Syringe Kit Includes (1) 90" Y-coiled tubing (1) large spike (1) small spike

ECOMED SOLUTIONS, LLC

Angiography kit

• Primary Device ID: 10855009006105
• NIH Device Record Key: 616b8edc-94f0-42ac-a149-8554a2094487
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Ecomed Angiographic
• Version Model Number: 128-200301
• Catalog Number: 128-200301
• 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: true
• 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

• Length: 90 Inch
• Length: 90 Inch

Operating and Storage Conditions

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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00855009006108 [Primary]
GS1	10855009006105 [Package]; Contains: 00855009006108; 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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