Impulse 7000DP

FDA UDI

Class II (US FDA UDI)

by Fluke Electronics Corporation

Identity

Trade Name: Impulse 7000DP FDA UDI
Generic Name: External defibrillator tester FDA UDI
Device Name: Defibrilator/AED Tester, External Pacer Analyzer FDA UDI
Model / Reference: IMPULSE 7000DP FDA UDI
Description: Defibrilator/AED Tester, External Pacer Analyzer FDA UDI

Identifiers

Catalog Number: 2811919 FDA UDI
Primary DI / UDI-DI: 00850540007126 FDA UDI
FDA Product Code: DRL FDA UDI
GMDN Term: External defibrillator tester FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 870.5325 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: External defibrillator tester

Impulse 7000DP by Fluke Electronics Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Fluke Electronics Corporation

Sources (1)

FDA UDI d4d9a663-6037-4833-9d22-83c9fcb15861 35 fields · synced May 30, 2026