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Vent 800-Emvp-24-01

by Zoll Medical Corporation

Vent 800-Emvp-24-01 is a Class II device made by Zoll Medical Corporation, listed in FDA GUDID since 8 Jul 2024 (UDI-DI 00847946094621), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00847946094621 UDI-DI Date8 Jul 2024ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Vent
Generic name
Transport electric ventilator
Model / reference
800-EMVP-24-01
Primary DI / UDI-DI
00847946094621
FDA product code
CBK, DQA
GMDN term
Transport electric ventilator
Device class
Class II
Regulation number
868.5895, 870.2700
GUDID distribution status
In Commercial Distribution
MRI safety
MR Conditional

Related devices

Category: Transport electric ventilator

Similar devices in this category

Other devices filed under Transport electric ventilator.

Other devices from Zoll Medical Corporation

See all devices from Zoll Medical Corporation →

Properties

  • Prescription use
  • Serial number
Other properties (13, all answered No)