FDA UDI In Commercial Distribution 🇺🇸 United States

MediChoice

DI: 20885632398176 · Model: 49993 · OWENS & MINOR DISTRIBUTION, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
50

Basic Information

Brand Name
MediChoice
Primary DI
20885632398176
Version / Model
49993
Company Name
OWENS & MINOR DISTRIBUTION, INC.
Labeler DUNS
007941230
Distribution Status
In Commercial Distribution
Device Count in Pkg
50
Record Status
Published
Publish Date
2023-09-14
Public Version
1
Public Version Date
2023-09-22
Public Version Status
New
Public Device Record Key
468408d6-bb81-48e8-a71b-7a76c24ce974

Device Description

ECG Electrode Monitoring Radiolucent Foam White 50/Pack CA/1000 Not Made with Natural Rubber Latex MediChoice

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
Yes
PM Exempt
Yes
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
DRX Electrode, electrocardiograph

GMDN Terms

Code Name
35035 Electrocardiographic electrode, single-use

Identifiers

Type ID
Package 30885632398173
Primary 20885632398176
Unit of Use 10885632398179

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
5 – 30 Degrees Celsius