FDA UDI Not in Commercial Distribution 🇺🇸 United States

CardioSens/Ultra II

DI: 10812345024682 · Model: 047029-00 · MORTARA INSTRUMENT, INC.
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
100

Basic Information

Brand Name
CardioSens/Ultra II
Primary DI
10812345024682
Version / Model
047029-00
Company Name
MORTARA INSTRUMENT, INC.
Labeler DUNS
062046149
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2016-09-24
Public Version
4
Public Version Date
2023-03-08
Public Version Status
Update
Public Device Record Key
fbc67a37-62b2-4c88-8f08-d39079380283
Distribution End Date
2023-03-07

Device Description

Electrodes

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
DRX Electrode, Electrocardiograph

GMDN Terms

Code Name
35035 Electrocardiographic electrode, single-use

Identifiers

Type ID
Package 30812345024686
Package 20812345024689
Primary 10812345024682
Unit of Use 00812345024682

Customer Contacts

Phone
888-667-8272

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
– 77 Degrees Fahrenheit