FDA UDI In Commercial Distribution 🇺🇸 United States

Monoject

DI: 10884521082892 · Model: 8881202017 · Cardinal Health, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
100

Basic Information

Brand Name
Monoject
Primary DI
10884521082892
Version / Model
8881202017
Catalog Number
8881202017
Company Name
Cardinal Health, Inc.
Labeler DUNS
080935429
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2016-09-24
Public Version
8
Public Version Date
2020-10-12
Public Version Status
Update
Public Device Record Key
5965c955-5387-4890-ac9c-9d4fb4fc9cce

Device Description

Blunt Cannula

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FMI Needle, hypodermic, single lumen

GMDN Terms

Code Name
33963 Peripheral intravenous catheterization support kit

Identifiers

Type ID
Package 20884521082899
Primary 10884521082892
Unit of Use 30884521082896

Customer Contacts

Device Sizes

Type Value Unit Text
Length 1 Inch
Device Size Text, specify Needle Gauge,18,Gauge;

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep dry;AVOID DIRECT SUNLIGHT