FDA UDI In Commercial Distribution 🇺🇸 United States

myCordella Patient App

DI: 00850008997037 · Model: 100256-02 · Endotronix, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
myCordella Patient App
Primary DI
00850008997037
Version / Model
100256-02
Company Name
Endotronix, Inc.
Labeler DUNS
806850835
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-08-13
Public Version
2
Public Version Date
2026-03-17
Public Version Status
Update
Public Device Record Key
0996a708-0aae-4d9e-9f96-f7995d9e82ba

Device Description

myCordella Patient App is a component of the myCordella Patient Kit. myCordella Patient App is an intuitive, user-friendly software that assists patients with obtaining vital sign measurements. • Collects & securely transmits daily health information to clinicians • Facilitates review of past measurements • Allows secure communication between patient and clinician

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
Yes
Has Serial Number
No
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
OEZ Cardiovascular Procedure Kit

GMDN Terms

Code Name
66386 Bedside monitor remote-viewing software, physiological parameter

Identifiers

Type ID
Primary 00850008997037

Customer Contacts