FDA UDI In Commercial Distribution 🇺🇸 United States

AED PRO

DI: 00847946097684 · Model: 91810200499991010 · Zoll Medical Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AED PRO
Primary DI
00847946097684
Version / Model
91810200499991010
Company Name
Zoll Medical Corporation
Labeler DUNS
055363428
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-03-28
Public Version
2
Public Version Date
2026-02-10
Public Version Status
Update
Public Device Record Key
08e7d14e-495e-489b-87ff-4a22c6218267

Device Description

AED PRO, SEMI-AUTO W/MNL OVERRIDE, (1 CPR-D PAD), ENG, PLUSTRAC1G

Device Characteristics

Single Use
No
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
MR Unsafe
Direct Marking Exempt
Yes
PM Exempt
No
Has Serial Number
Yes
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
48048 Rechargeable professional automated external defibrillator

Identifiers

Type ID
Primary 00847946097684

Storage Conditions

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
Type
Storage Environment Humidity
Temperature Range
0 – 0 Percent (%) Relative Humidity