FDA UDI In Commercial Distribution 🇺🇸 United States

MaxPlus

DI: 50885403427976 · Model: MPX9102-SF-C · CAREFUSION 303, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
50

Basic Information

Brand Name
MaxPlus
Primary DI
50885403427976
Version / Model
MPX9102-SF-C
Catalog Number
MPX9102-SF-C
Company Name
CAREFUSION 303, INC.
Labeler DUNS
360624720
Distribution Status
In Commercial Distribution
Device Count in Pkg
50
Record Status
Published
Publish Date
2016-11-04
Public Version
4
Public Version Date
2020-04-27
Public Version Status
Update
Public Device Record Key
d3382c81-3a4e-4781-85d7-d753480a22ef

Device Description

MaxPlus ectension set with needleless connector and Y-site

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
Yes
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 20885403427975
Primary 50885403427976
Unit of Use 10885403427978

Customer Contacts

Storage Conditions

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