FDA UDI In Commercial Distribution 🇺🇸 United States

Alaris

DI: 10885403234194 · Model: 10373772 · CAREFUSION 303, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Alaris
Primary DI
10885403234194
Version / Model
10373772
Catalog Number
10373772
Company Name
CAREFUSION 303, INC.
Labeler DUNS
360624720
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-22
Public Version
5
Public Version Date
2022-01-17
Public Version Status
Update
Public Device Record Key
b07045ad-f99a-432e-b1e1-a85e5e103fc7

Device Description

EXT SMALLBORE 6 INCHES

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
Primary 10885403234194
Package 50885403234192

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Room Temperature