BD Vacutainer® SST™ II Advance 367953

GUDID 50382903679534

BD Vacutainer® SST™ II Advance

Becton, Dickinson U.K. Limited

Evacuated blood collection tube IVD, clot activator/gel separator Evacuated blood collection tube IVD, clot activator/gel separator Evacuated blood collection tube IVD, clot activator/separator Evacuated blood collection tube IVD, clot activator/separator Evacuated blood collection tube IVD, clot activator/separator Evacuated blood collection tube IVD, clot activator/separator Evacuated blood collection tube IVD, clot activator/separator Evacuated blood collection tube IVD, clot activator/separator Evacuated blood collection tube IVD, clot activator/separator Evacuated blood collection tube IVD, clot activator/separator Evacuated blood collection tube IVD, clot activator/separator Evacuated blood collection tube IVD, clot activator/separator Evacuated blood collection tube IVD, clot activator/separator Evacuated blood collection tube IVD, clot activator/separator Evacuated blood collection tube IVD, clot activator/separator Evacuated blood collection tube IVD, clot activator/separator Evacuated blood collection tube IVD, clot activator/separator

• Primary Device ID: 50382903679534
• NIH Device Record Key: ae433d69-33d2-4a8c-8bf5-db4bd6fd5250
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BD Vacutainer® SST™ II Advance
• Version Model Number: 367953
• Catalog Number: 367953
• Company DUNS: 225931062
• Company Name: Becton, Dickinson U.K. Limited
• Device Count: 1000
• DM Exempt: true
• 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	00382903679539 [Unit of Use]
GS1	50382903679534 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• BK050036

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: 2016-08-22

On-Brand Devices [BD Vacutainer® SST™ II Advance]

• 50382903679572: BD Vacutainer® SST™ II Advance
• 50382903679558: BD Vacutainer® SST™ II Advance
• 50382903679534: BD Vacutainer® SST™ II Advance
• 50382903668828: BD Vacutainer® SST™ II Advance
• 50382903664448: BD Vacutainer® SST™ II Advance