BD Eclipse 305769

GUDID 50382903057691

NEEDLE ECLIPSE 23X1-1/4 RB

BECTON, DICKINSON AND COMPANY

Hypodermic needle, single-use

• Primary Device ID: 50382903057691
• NIH Device Record Key: 9f268908-7254-47d1-9b2f-e7f8b1a88a4b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BD Eclipse
• Version Model Number: 305769
• Catalog Number: 305769
• Company DUNS: 001292192
• Company Name: BECTON, DICKINSON AND COMPANY
• Device Count: 100
• DM Exempt: true
• 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

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Room Temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room Temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room Temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room Temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room Temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room Temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room Temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room Temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room Temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room Temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room Temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room Temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room Temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room Temperature
• Special Storage Condition, Specify: Between 0 and 0 *Room Temperature

Device Identifiers

Device Issuing Agency	Device ID
GS1	00382903057696 [Unit of Use]
GS1	30382903057697 [Primary]
GS1	50382903057691 [Package]; Contains: 30382903057697; Package: Case [12 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K010188

FDA Product Code

• FMI: Needle, hypodermic, single lumen

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: 2019-10-23
• Device Publish Date: 2016-09-16

On-Brand Devices [BD Eclipse]

• 50382903057691: NEEDLE ECLIPSE 23X1-1/4 RB
• 50382903057684: NEEDLE ECLIPSE 22X1 RB
• 50382903057677: NEEDLE ECLIPSE 25X1-1/2 RB
• 50382903057660: NEEDLE ECLIPSE 18X1-1/2 RB
• 50382903057653: NEEDLE ECLIPSE 21X1-1/2 RB TW
• 50382903057646: NEEDLE ECLIPSE 21X1 RB TW
• 50382903057639: NEEDLE ECLIPSE 22X1-1/2 RB
• 50382903057622: NEEDLE ECLIPSE 23X1 RB
• 50382903057615: NEEDLE ECLIPSE 25X1 RB
• 50382903057592: NEEDLE ECLIPSE 25X5/8
• 50382903057585: NEEDLE ECLIPSE 27X1/2
• 50382903057578: NEEDLE ECLIPSE 30X1/2