FDA UDI In Commercial Distribution 🇺🇸 United States

Powerheart® Adult Defibrillation Pads

DI: 00812394020591 · Model: 2019199-002 · Cardiac Science Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Powerheart® Adult Defibrillation Pads
Primary DI
00812394020591
Version / Model
2019199-002
Catalog Number
2019199-002
Company Name
Cardiac Science Corporation
Labeler DUNS
190713797
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-07-24
Public Version
3
Public Version Date
2023-07-06
Public Version Status
Update
Public Device Record Key
9b1d78da-8e03-43c4-87d4-ca85794e627e

Device Description

Defibrillation Pads(adult) with two-year shelf life for full range of Powerheart® AEDs, under GE part number

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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
MKJ Automated External Defibrillators (Non-Wearable)

GMDN Terms

Code Name
44771 External defibrillation electrode, adult, single-use

Identifiers

Type ID
Primary 00812394020591

Storage Conditions

Type
Handling Environment Temperature
Temperature Range
0 – 50 Degrees Celsius
Type
Storage Environment Temperature
Temperature Range
0 – 50 Degrees Celsius