FDA UDI In Commercial Distribution 🇺🇸 United States

N/A

DI: 70885403287048 · Model: 2009101-404 · Carefusion Finland 320 Oy
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
3

Basic Information

Brand Name
N/A
Primary DI
70885403287048
Version / Model
2009101-404
Catalog Number
2009101-404
Company Name
Carefusion Finland 320 Oy
Labeler DUNS
367919120
Distribution Status
In Commercial Distribution
Device Count in Pkg
3
Record Status
Published
Publish Date
2016-09-22
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
dfef4c9f-9d97-4fef-969c-5c7936d09248

Device Description

ECG Electrodes, 55mm Round, Clear Tape, Hydrogel

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
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 50885403287044
Primary 70885403287048
Unit of Use 10885403287046

Customer Contacts

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
14 – 104 Degrees Fahrenheit