Eclipse 305887

GUDID 30382903058878

NEEDLE ECLIPSE S/T 22X1-1/4 RB

BECTON, DICKINSON AND COMPANY

Hypodermic needle, single-use

• Primary Device ID: 30382903058878
• NIH Device Record Key: b0d24c93-8406-4918-bb58-59a0380eca42
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Eclipse
• Version Model Number: 305887
• Catalog Number: 305887
• 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	00382903058877 [Primary]
GS1	30382903058878 [Package]; Contains: 00382903058877; Package: Shelfpack [100 Units]; In Commercial Distribution
GS1	50382903058872 [Package]; Package: Case [12 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K100209

FDA Product Code

• FMI: Needle, hypodermic, single lumen

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: 2023-09-01

On-Brand Devices [Eclipse]

• 50382903058957: NEEDLE ECLIPSE S/T 21X1-1/2 RB TW
• 50382903058926: NEEDLE ECLIPSE S/T 23X1 RB
• 30382903058878: NEEDLE ECLIPSE S/T 22X1-1/4 RB
• 50382903057714: NEEDLE ECLIPSE S/T 30X1/2 RB
• 30382903057703: NEEDLE ECLIPSE S/T 27X1/2 RB
• 30382903033066: SYRINGE 3ML LL ECLIPSE 23X1-1/2 RB TW
• 30382903024378: NEEDLE 18X1-1/2 ECLIPSE