BD Microtainer® Tubes with LH (Lithium Heparin) 365965

GUDID 50382903659659

BD Microtainer® Tubes with LH (Lithium Heparin)

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: 50382903659659
• NIH Device Record Key: 54312e4f-b891-4b85-a793-99e3a233ab5c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BD Microtainer® Tubes with LH (Lithium Heparin)
• Version Model Number: 365965
• Catalog Number: 365965
• Company DUNS: 001292192
• Company Name: BECTON, DICKINSON AND COMPANY
• Device Count: 200
• 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	00382903659654 [Unit of Use]
GS1	50382903659659 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K991702

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 Microtainer® Tubes with LH (Lithium Heparin)]

• 50382903659659: BD Microtainer® Tubes with LH (Lithium Heparin)
• 30382903659655: BD Microtainer® Tubes with LH (Lithium Heparin)