FDA UDI In Commercial Distribution 🇺🇸 United States

MaxPlus

DI: 10885403237218 · Model: MPX5300-C · BD Switzerland Sàrl
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
MaxPlus
Primary DI
10885403237218
Version / Model
MPX5300-C
Catalog Number
MPX5300-C
Company Name
BD Switzerland Sàrl
Labeler DUNS
482631558
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-22
Public Version
6
Public Version Date
2025-07-04
Public Version Status
Update
Public Device Record Key
5d9466f6-72f1-4e07-96c7-9e5818e5de7f

Device Description

Pressure rated extension set, with clear needleless connector and Y-Site 23 cm (9 in)

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
Primary 10885403237218
Package 50885403237216

Customer Contacts

Device Sizes

Type Value Unit Text
Length 9 Inch

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-40 – 125 Degrees Fahrenheit
Type
Special Storage Condition, Specify
Special Conditions
Fragile, handle with care
Type
Special Storage Condition, Specify
Special Conditions
Keep away from sunlight
Type
Special Storage Condition, Specify
Special Conditions
Keep dry