BD PosiFlush™ 306499

GUDID 50382903064996

SYRINGE 10ML SHORT PR SALINE 10ML FILL

BECTON, DICKINSON AND COMPANY

Vascular catheter/cannula flush solution, non-anticoagulant, non-antimicrobial Vascular catheter/cannula flush solution, non-anticoagulant, non-antimicrobial Vascular catheter/cannula flush solution, non-anticoagulant, non-antimicrobial Vascular catheter/cannula flush solution, non-anticoagulant, non-antimicrobial Vascular catheter/cannula flush solution, non-anticoagulant, non-antimicrobial Vascular catheter/cannula flush solution, non-anticoagulant, non-antimicrobial Vascular catheter/cannula flush solution, non-anticoagulant, non-antimicrobial Vascular catheter/cannula flush solution, non-anticoagulant, non-antimicrobial Vascular catheter/cannula flush solution, non-anticoagulant, non-antimicrobial Vascular catheter/cannula flush solution, non-anticoagulant, non-antimicrobial Vascular catheter/cannula flush solution, non-anticoagulant, non-antimicrobial Vascular catheter/cannula flush solution, non-anticoagulant, non-antimicrobial Vascular catheter/cannula flush solution, non-anticoagulant, non-antimicrobial Vascular catheter/cannula flush solution, non-anticoagulant, non-antimicrobial Vascular catheter/cannula flush solution, non-anticoagulant, non-antimicrobial Vascular catheter/cannula flush solution, non-anticoagulant, non-antimicrobial

• Primary Device ID: 50382903064996
• NIH Device Record Key: f208fb26-7db1-4951-8a04-caabd03221c1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BD PosiFlush™
• Version Model Number: 306499
• Catalog Number: 306499
• Company DUNS: 001292192
• Company Name: BECTON, DICKINSON AND COMPANY
• Device Count: 30
• 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

Operating and Storage Conditions

• Storage Environment Temperature: Between 20 Degrees Celsius and 25 Degrees Celsius
• Storage Environment Temperature: Between 20 Degrees Celsius and 25 Degrees Celsius
• Storage Environment Temperature: Between 20 Degrees Celsius and 25 Degrees Celsius
• Storage Environment Temperature: Between 20 Degrees Celsius and 25 Degrees Celsius
• Storage Environment Temperature: Between 20 Degrees Celsius and 25 Degrees Celsius
• Storage Environment Temperature: Between 20 Degrees Celsius and 25 Degrees Celsius
• Storage Environment Temperature: Between 20 Degrees Celsius and 25 Degrees Celsius
• Storage Environment Temperature: Between 20 Degrees Celsius and 25 Degrees Celsius
• Storage Environment Temperature: Between 20 Degrees Celsius and 25 Degrees Celsius
• Storage Environment Temperature: Between 20 Degrees Celsius and 25 Degrees Celsius
• Storage Environment Temperature: Between 20 Degrees Celsius and 25 Degrees Celsius
• Storage Environment Temperature: Between 20 Degrees Celsius and 25 Degrees Celsius
• Storage Environment Temperature: Between 20 Degrees Celsius and 25 Degrees Celsius
• Storage Environment Temperature: Between 20 Degrees Celsius and 25 Degrees Celsius
• Storage Environment Temperature: Between 20 Degrees Celsius and 25 Degrees Celsius
• Storage Environment Temperature: Between 20 Degrees Celsius and 25 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
GS1	00382903064991 [Unit of Use]
GS1	30382903064992 [Primary]
GS1	50382903064996 [Package]; Contains: 30382903064992; Package: Case [16 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K161552

FDA Product Code

• NGT: Saline, vascular access flush

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-09-09
• Device Publish Date: 2022-09-01

On-Brand Devices [BD PosiFlush™]

• 50382903064934: SYRINGE 10ML SHORT PR SALINE 3ML FILL
• 50382903064996: SYRINGE 10ML SHORT PR SALINE 10ML FILL