FDA UDI Not in Commercial Distribution 🇺🇸 United States

PRO PADZ

DI: 00847946016463 · Model: 8900-4006 · Zoll Medical Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
PRO PADZ
Primary DI
00847946016463
Version / Model
8900-4006
Company Name
Zoll Medical Corporation
Labeler DUNS
055363428
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-09-24
Public Version
6
Public Version Date
2026-02-16
Public Version Status
Update
Public Device Record Key
d92ef901-aa99-4883-918f-107d428fb87f
Distribution End Date
2026-01-01

Device Description

PRO*PADZ SOLID GEL RADIOLUCENT MULTI-FUNCTION ELECTRODES - 1 PAIR

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
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
DTE PULSE-GENERATOR, PACEMAKER, EXTERNAL

GMDN Terms

Code Name
48048 Rechargeable professional automated external defibrillator

Identifiers

Type ID
Primary 00847946016463

Device Sizes

Type Value Unit Text
Device Size Text, specify 14.1" X 9.1" X 1.0"

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
0 – 35 Degrees Celsius
Type
Handling Environment Temperature
Temperature Range
0 – 50 Degrees Celsius