BD Eclipse, BD Luer-Lok 303321

GUDID 50382903033213

SYR 10ML LL W/NDL ECLIPSE 21X1-1/2 RB TW

BECTON, DICKINSON AND COMPANY

General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle

• Primary Device ID: 50382903033213
• NIH Device Record Key: 55983d7c-8a19-486c-84e9-64c2dcc8a7aa
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BD Eclipse, BD Luer-Lok
• Version Model Number: 303321
• Catalog Number: 303321
• Company DUNS: 001292192
• Company Name: BECTON, DICKINSON AND COMPANY
• 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: true
• 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	00382903033218 [Primary]
GS1	30382903033219 [Package]; Contains: 00382903033218; Package: Shelfpack [50 Units]; In Commercial Distribution
GS1	50382903033213 [Package]; Contains: 30382903033219; Package: Case [6 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K161170

FDA Product Code

• FMF: Syringe, piston

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: 2023-09-11
• Device Publish Date: 2023-09-02

On-Brand Devices [BD Eclipse, BD Luer-Lok]

• 50382903033213: SYR 10ML LL W/NDL ECLIPSE 21X1-1/2 RB TW
• 30382903033073: SYRINGE 5ML LL 23X1-1/2IN ECLIPSE RB TW