BD Epilor 405291

GUDID 50382904052916

SYRINGE EPILOR PLASTIC LOR 7ML LL S/SU

BECTON, DICKINSON AND COMPANY

Low-resistance syringe

• Primary Device ID: 50382904052916
• NIH Device Record Key: 8c1f3b19-31e4-4c83-9ecc-4f9ccfeede3e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BD Epilor
• Version Model Number: 405291
• Catalog Number: 405291
• Company DUNS: 001292192
• Company Name: BECTON, DICKINSON AND COMPANY
• Device Count: 10
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00382904052911 [Unit of Use]
GS1	30382904052912 [Primary]
GS1	50382904052916 [Package]; Contains: 30382904052912; Package: Case [5 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K210983
• Premarket Notification: K925902

FDA Product Code

• CAZ: Anesthesia conduction kit

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-16

On-Brand Devices [BD Epilor]

• 50382904052923: SYRINGE EPILOR PLASTIC LOR 7ML LS S/SU
• 50382904052916: SYRINGE EPILOR PLASTIC LOR 7ML LL S/SU