Vesco Medical 5mL ENFit Amber Syringe

GUDID 10850801006926

5mL ENFit Amber Syringe

Vesco Medical, LLC

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• Primary Device ID: 10850801006926
• NIH Device Record Key: e922563e-0f54-4aec-bb76-f0bf7f0b2e4c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Vesco Medical 5mL ENFit Amber Syringe
• Version Model Number: VED-605AB
• Company DUNS: 119007223
• Company Name: Vesco Medical, LLC
• 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: false
• 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: 6149145991
• Email: info@vescomedical.com
• Phone: 6149145991
• Email: info@vescomedical.com
• Phone: 6149145991
• Email: info@vescomedical.com
• Phone: 6149145991
• Email: info@vescomedical.com
• Phone: 6149145991
• Email: info@vescomedical.com
• Phone: 6149145991
• Email: info@vescomedical.com
• Phone: 6149145991
• Email: info@vescomedical.com
• Phone: 6149145991
• Email: info@vescomedical.com
• Phone: 6149145991
• Email: info@vescomedical.com
• Phone: 6149145991
• Email: info@vescomedical.com
• Phone: 6149145991
• Email: info@vescomedical.com
• Phone: 6149145991
• Email: info@vescomedical.com
• Phone: 6149145991
• Email: info@vescomedical.com
• Phone: 6149145991
• Email: info@vescomedical.com
• Phone: 6149145991
• Email: info@vescomedical.com
• Phone: 6149145991
• Email: info@vescomedical.com
• Phone: 6149145991
• Email: info@vescomedical.com
• Phone: 6149145991
• Email: info@vescomedical.com

Device Dimensions

• Total Volume: 5 Milliliter
• Total Volume: 5 Milliliter
• Total Volume: 5 Milliliter
• Total Volume: 5 Milliliter
• Total Volume: 5 Milliliter
• Total Volume: 5 Milliliter
• Total Volume: 5 Milliliter
• Total Volume: 5 Milliliter
• Total Volume: 5 Milliliter
• Total Volume: 5 Milliliter
• Total Volume: 5 Milliliter
• Total Volume: 5 Milliliter
• Total Volume: 5 Milliliter
• Total Volume: 5 Milliliter
• Total Volume: 5 Milliliter
• Total Volume: 5 Milliliter
• Total Volume: 5 Milliliter
• Total Volume: 5 Milliliter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850801006929 [Primary]
GS1	10850801006926 [Package]; Contains: 00850801006929; Package: Inner Pack [250 Units]; In Commercial Distribution
GS1	20850801006923 [Package]; Package: Case [4 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K190502

FDA Product Code

• PNR: Enteral Syringes With Enteral Specific Connectors

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-06-13
• Device Publish Date: 2023-06-05

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