FDA UDI In Commercial Distribution 🇺🇸 United States

MaxGuard

DI: 50885403237438 · Model: MV0700 · CAREFUSION 303, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
100

Basic Information

Brand Name
MaxGuard
Primary DI
50885403237438
Version / Model
MV0700
Catalog Number
MV0700
Company Name
CAREFUSION 303, INC.
Labeler DUNS
360624720
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2016-09-22
Public Version
5
Public Version Date
2021-02-19
Public Version Status
Update
Public Device Record Key
7ca3f7fb-b880-475f-8911-1041409990ba

Device Description

MaxGuard multidose vial adaptor

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
43324 Fluid transfer set, general-purpose

Identifiers

Type ID
Primary 50885403237438
Unit of Use 10885403237430

Customer Contacts

Storage Conditions

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