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CloudHRV™ System 68481

by Inmedix, Inc.

Listed FDA GUDID listing, not in commercial distribution

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 23 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberG697684810 UDI-DI Date14 Feb 2025ListedStatusListed GUDID: not in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
CloudHRV™ System
Generic Name
Electrocardiograph, professional, multichannel
Model / Ref / Catalog
68481
Primary DI / UDI-DI
G697684810
510(k) Number
FDA Product Code
DPS
GMDN Term
Electrocardiograph, professional, multichannel
Device Class
Class II
Regulation Number
870.2340
GUDID distribution status
Not in Commercial Distribution

Related devices

Category: Electrocardiograph, professional, multichannel

Cleared under the same submission (K241217)

Other devices from Inmedix, Inc.

Properties

  • Prescription Use
  • Serial Number
  • Manufacturing Date

Other properties (11)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Lot / Batch Number: No
  • Expiration Date: No