FDA UDI In Commercial Distribution 🇺🇸 United States

Texium

DI: 50885403221680 · Model: MY8020 · CAREFUSION 303, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
100

Basic Information

Brand Name
Texium
Primary DI
50885403221680
Version / Model
MY8020
Catalog Number
MY8020
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
2021-11-29
Public Version Status
Update
Public Device Record Key
13234585-ca9b-4202-996b-947a9ab9ac98

Device Description

Texium Needle-Free Syringe

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
FMF Syringe, piston

GMDN Terms

Code Name
47017 General-purpose syringe, single-use

Identifiers

Type ID
Primary 50885403221680
Unit of Use 10885403221682

Customer Contacts

Storage Conditions

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