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Z Vent

FDA UDI

Class II (US FDA UDI)

by Zoll Medical Corporation

Identity

Trade Name
Z Vent FDA UDI
Generic Name
Transport electric ventilator FDA UDI
Device Name
MAIN ASSEMBLY, VENTILATOR, EMV+, MRI, REFURBISHED FDA UDI
Model / Reference
799-EMVP-05-01-66 FDA UDI
Description
MAIN ASSEMBLY, VENTILATOR, EMV+, MRI, REFURBISHED FDA UDI

Identifiers

Primary DI / UDI-DI
00812394023455 FDA UDI
FDA Product Code
DQA FDA UDI
CBK FDA UDI
GMDN Term
Transport electric ventilator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2700 FDA UDI
868.5895 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
MRI Safety
MR Safe FDA UDI

Category: Transport electric ventilator

Z Vent by Zoll Medical Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Transport electric ventilator.

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 deb0d5b4-620d-47c3-9542-08aac23960b9 34 fields · synced Jun 8, 2026