Alaris

Basic Information

• Brand Name: Alaris
• Primary DI: 50885403460232
• Version / Model: 30893-07
• Catalog Number: 30893-07
• Company Name: CAREFUSION 303, INC.
• Labeler DUNS: 360624720
• Distribution Status: In Commercial Distribution
• Device Count in Pkg: 50
• Record Status: Published
• Publish Date: 2017-08-08
• Public Version: 4
• Public Version Date: 2020-04-27
• Public Version Status: Update
• Public Device Record Key: bb3b28dd-3280-438e-81b3-38103ad44283

Device Description

PCEA ASV YELLOW MICROBORE

Device Characteristics

• Single Use: Yes
• Prescription Use (Rx): Yes
• Over the Counter (OTC): No
• Kit: No
• Combination Product: No
• HCT/P: No
• Contains NRL: No
• Not Made with NRL: No
• MRI Safety: Labeling does not contain MRI Safety Information
• Direct Marking Exempt: No
• PM Exempt: No
• Has Serial Number: No
• Has Lot/Batch Number: Yes
• Has Manufacturing Date: No
• Has Expiration Date: Yes
• Has Donation ID: No

Sterilization

• Is Sterile: Yes
• Sterilization Prior Use: No

Product Codes

Code	Name	Medical Specialty	Regulation #	Device Class
FPA	Set, administration, intravascular	General Hospital	880.5440	2

GMDN Terms

Code	Name	Definition	Implantable	Status
41477	Patient-controlled analgesia electric infusion pump administration set	A collection of sterile devices that typically consists of a reservoir (e.g., a syringe or plastic pouch), plastic tubing, a check valve, and Luer connectors, designed for the controlled intravenous (IV) administration of opioid pain medication using an electrically-powered, patient-controlled analgesia (PCA) infusion pump. This is a single-use device.	No	Active

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Primary	50885403460232	GS1
Unit of Use	10885403460234	GS1

Customer Contacts

• Phone: [phone]
• Email: [email protected]

Storage Conditions

• Type: Special Storage Condition, Specify
• Special Conditions: Room Temperature