FDA UDI In Commercial Distribution 🇺🇸 United States

Monoject

DI: 20192253035152 · Model: 8881120037 · Cardinal Health 200, LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
50

Basic Information

Brand Name
Monoject
Primary DI
20192253035152
Version / Model
8881120037
Catalog Number
8881120037
Company Name
Cardinal Health 200, LLC
Labeler DUNS
961027315
Distribution Status
In Commercial Distribution
Device Count in Pkg
50
Record Status
Published
Publish Date
2023-06-26
Public Version
1
Public Version Date
2023-07-04
Public Version Status
New
Public Device Record Key
b6eac5e3-d809-4c59-a034-685c75a0f40c

Device Description

20 mL Syringe Regular Tip

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
No
Sterilization Prior Use
No

Product Codes

Code Name
FMF Syringe, piston

GMDN Terms

Code Name
47017 General-purpose syringe, single-use

Identifiers

Type ID
Package 50192253035153
Primary 20192253035152
Unit of Use 10192253035155