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Aed Pro

FDA UDI

Class III (US FDA UDI)

by Zoll Medical Corporation

Identity

Trade Name
AED PRO FDA UDI
Generic Name
Non-rechargeable professional semi-automated external defibrillator FDA UDI
Device Name
AED PRO, SEMI AUTO ONLY, NO BATTERY, VOICE, LCD, ENGLISH FDA UDI
Model / Reference
90110402499991010 FDA UDI
Description
AED PRO, SEMI AUTO ONLY, NO BATTERY, VOICE, LCD, ENGLISH FDA UDI

Identifiers

Primary DI / UDI-DI
00847946096892 FDA UDI
FDA Product Code
MKJ FDA UDI
GMDN Term
Non-rechargeable professional semi-automated external defibrillator FDA UDI

Classification

Device Class
Class III FDA UDI
Regulation Number
870.5310 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Non-rechargeable professional semi-automated external defibrillator

Aed Pro by Zoll Medical Corporation — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Non-rechargeable professional semi-automated external defibrillator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Zoll Medical Corporation

Sources (1)

  • FDA UDI a8d95cc3-7cd8-4e63-8e0e-06b8198b313f 34 fields · synced Jun 6, 2026