SYRINGE 20ML E/T 300613

GUDID 00382903006137

SYRINGE 20ML E/T

BECTON DICKINSON & COMPANY LTD

General-purpose syringe, single-use

• Primary Device ID: 00382903006137
• NIH Device Record Key: 1d10d068-44c2-4c09-aef8-8fc669130d38
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SYRINGE 20ML E/T
• Version Model Number: 300613
• Catalog Number: 300613
• Company DUNS: 989811195
• Company Name: BECTON DICKINSON & COMPANY LTD
• Device Count: 1
• 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 [Primary]
GS1	30382903006138 [Package]; Package: Shelfpack [120 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: 5
• Public Version Date: 2024-04-26
• Device Publish Date: 2016-09-19

Devices Manufactured by BECTON DICKINSON & COMPANY LTD

• 00382903006137 - SYRINGE 20ML E/T: 2024-04-26SYRINGE 20ML E/T
• 00382903006137 - SYRINGE 20ML E/T: 2024-04-26 SYRINGE 20ML E/T
• 50382903006132 - N/A: 2018-10-01 SYRINGE 20ML E/T
• 50382903008662 - N/A: 2018-10-01 SYRINGE 60ML E/T