BD Vacutainer® 365047

GUDID 50382903650472

BD Vacutainer® Barricor™ Lithium HeparinN Plasma Tubes

Becton, Dickinson U.K. Limited

Evacuated blood collection tube IVD, lithium heparin/mechanical separator Evacuated blood collection tube IVD, lithium heparin/mechanical separator Evacuated blood collection tube IVD, anticoagulant/separator Evacuated blood collection tube IVD, anticoagulant/separator Evacuated blood collection tube IVD, anticoagulant/separator Evacuated blood collection tube IVD, anticoagulant/separator Evacuated blood collection tube IVD, anticoagulant/separator Evacuated blood collection tube IVD, anticoagulant/separator Evacuated blood collection tube IVD, anticoagulant/separator Evacuated blood collection tube IVD, anticoagulant/separator Evacuated blood collection tube IVD, anticoagulant/separator Evacuated blood collection tube IVD, anticoagulant/separator Evacuated blood collection tube IVD, anticoagulant/separator Evacuated blood collection tube IVD, anticoagulant/separator Evacuated blood collection tube IVD, anticoagulant/separator Evacuated blood collection tube IVD, anticoagulant/separator Evacuated blood collection tube IVD, anticoagulant/separator Evacuated blood collection tube IVD, anticoagulant/separator Evacuated blood collection tube IVD, anticoagulant/separator Evacuated blood collection tube IVD, anticoagulant/separator

• Primary Device ID: 50382903650472
• NIH Device Record Key: 0ee57acf-53d1-4a20-aeb9-e01939374c0f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BD Vacutainer®
• Version Model Number: 365047
• Catalog Number: 365047
• Company DUNS: 225931062
• Company Name: Becton, Dickinson U.K. Limited
• Device Count: 1000
• 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: 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	00382903650477 [Unit of Use]
GS1	50382903650472 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K160657

FDA Product Code

• JKA: Tubes, vials, systems, serum separators, blood collection

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-11-04

On-Brand Devices [BD Vacutainer®]

• 50382903650472: BD Vacutainer® Barricor™ Lithium HeparinN Plasma Tubes
• 50382903650465: BD Vacutainer® Barricor™ Lithium HeparinN Plasma Tubes
• 50382903650458: BD Vacutainer® Barricor™ Lithium HeparinN Plasma Tubes
• 50382903650441: BD Vacutainer® Barricor™ Lithium Heparin Plasma Tubes
• 50382903650434: BD Vacutainer® Barricor™ Lithium HeparinN Plasma Tubes