FDA UDI In Commercial Distribution 🇺🇸 United States

AED 3

DI: 00812394026661 · Model: 8501-001201-24-66 · Zoll Medical Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
AED 3
Primary DI
00812394026661
Version / Model
8501-001201-24-66
Company Name
Zoll Medical Corporation
Labeler DUNS
055363428
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-04-28
Public Version
2
Public Version Date
2025-06-16
Public Version Status
Update
Public Device Record Key
67ba02be-f0b3-4f4d-9ea5-6052f36e595a

Device Description

SEMI-AUTOMATIC, ZOLL AED 3, BRAZILIAN PORTUGUESE AHA, REFURB

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
No
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
MKJ Automated external defibrillators (non-wearable)

GMDN Terms

Code Name
47910 Non-rechargeable public semi-automated external defibrillator

Identifiers

Type ID
Primary 00812394026661

Storage Conditions

Type
Storage Environment Humidity
Temperature Range
0 – 0 Percent (%) Relative Humidity
Type
Storage Environment Atmospheric Pressure
Temperature Range
Low: 0 KiloPascal
Type
Handling Environment Temperature
Temperature Range
0 – 0 Degrees Celsius
Type
Storage Environment Temperature
Temperature Range
0 – 0 Degrees Celsius