FDA UDI In Commercial Distribution 🇺🇸 United States

MaxPlus

DI: 50885403230132 · Model: MP5302-C · CAREFUSION 303, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
50

Basic Information

Brand Name
MaxPlus
Primary DI
50885403230132
Version / Model
MP5302-C
Catalog Number
MP5302-C
Company Name
CAREFUSION 303, INC.
Labeler DUNS
360624720
Distribution Status
In Commercial Distribution
Device Count in Pkg
50
Record Status
Published
Publish Date
2016-09-22
Public Version
4
Public Version Date
2020-04-27
Public Version Status
Update
Public Device Record Key
061198e8-c40f-4138-86cf-1cb96b8447b4

Device Description

MaxPlus pressure rated extension set with needleless connector

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
FPA Set, administration, intravascular

GMDN Terms

Code Name
12170 Intravenous administration tubing extension set

Identifiers

Type ID
Package 20885403230131
Primary 50885403230132
Unit of Use 10885403230134

Customer Contacts

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-40 – 125 Degrees Fahrenheit