BD Vacutainer® PST™ Gel and Lithium Heparin 367964

GUDID 50382903679640

BD Vacutainer® PST™ Gel and Lithium Heparin 126 Units

BECTON, DICKINSON AND COMPANY

Non-evacuated blood collection tube IVD, lithium heparin/gel separator, non-sterile Non-evacuated blood collection tube IVD, lithium heparin/gel separator, non-sterile Non-evacuated blood collection tube IVD, anticoagulant/separator Non-evacuated blood collection tube IVD, anticoagulant/separator Non-evacuated blood collection tube IVD, anticoagulant/separator Non-evacuated blood collection tube IVD, anticoagulant/separator Non-evacuated blood collection tube IVD, anticoagulant/separator Non-evacuated blood collection tube IVD, anticoagulant/separator Non-evacuated blood collection tube IVD, anticoagulant/separator Non-evacuated blood collection tube IVD, anticoagulant/separator Non-evacuated blood collection tube IVD, anticoagulant/separator Non-evacuated blood collection tube IVD, anticoagulant/separator Non-evacuated blood collection tube IVD, anticoagulant/separator Non-evacuated blood collection tube IVD, anticoagulant/separator Non-evacuated blood collection tube IVD, anticoagulant/separator Non-evacuated blood collection tube IVD, anticoagulant/separator Non-evacuated blood collection tube IVD, anticoagulant/separator

• Primary Device ID: 50382903679640
• NIH Device Record Key: cbed6991-d846-4592-87e6-29dab2eb336b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BD Vacutainer® PST™ Gel and Lithium Heparin
• Version Model Number: 367964
• Catalog Number: 367964
• Company DUNS: 001292192
• Company Name: BECTON, DICKINSON AND COMPANY
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00382903679645 [Unit of Use]
GS1	50382903679640 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K945952

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: 2016-07-28

On-Brand Devices [BD Vacutainer® PST™ Gel and Lithium Heparin]

• 50382903679640: BD Vacutainer® PST™ Gel and Lithium Heparin 126 Units
• 50382903679619: BD Vacutainer® PST™ Gel and Lithium Heparin 65 Units
• 50382903679602: BD Vacutainer® PST™ Gel and Lithium Heparin (N) 56 Units