N/A 300613

GUDID 50382903006132

SYRINGE 20ML E/T

BECTON DICKINSON & COMPANY LTD

General-purpose syringe, single-use General-purpose syringe, single-use

• Primary Device ID: 50382903006132
• NIH Device Record Key: 1d10d068-44c2-4c09-aef8-8fc669130d38
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: N/A
• Version Model Number: 300613
• Catalog Number: 300613
• Company DUNS: 989811195
• Company Name: BECTON DICKINSON & COMPANY LTD
• Device Count: 120
• 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	00382903006137 [Unit of Use]
GS1	30382903006138 [Primary]
GS1	50382903006132 [Package]; Contains: 30382903006138; Package: Case [4 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K110771

FDA Product Code

• FMF: Syringe, piston

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2018-10-01
• Device Publish Date: 2016-09-19

On-Brand Devices [N/A]

• 50382903008662: SYRINGE 60ML E/T
• 50382903006132: SYRINGE 20ML E/T