← Back to catalogue

Aed 3

FDA UDI

Class III (US FDA UDI)

by Zoll Medical Corporation

Identity

Trade Name
AED 3 FDA UDI
Generic Name
Non-rechargeable professional semi-automated external defibrillator FDA UDI
Device Name
BLS, ZOLL AED 3, USB, ENGLISH UK ERC FDA UDI
Model / Reference
1128-001209-07 FDA UDI
Description
BLS, ZOLL AED 3, USB, ENGLISH UK ERC FDA UDI

Identifiers

Primary DI / UDI-DI
00847946047290 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 3 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Zoll Medical Corporation

Sources (1)

  • FDA UDI 8c47ff25-9a8c-43cb-9979-c4993053c05a 34 fields · synced Jun 8, 2026