Skip to content

Aermos Aermos System

by Scottcare Corporation, the

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 22 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00856298006411 UDI-DI Date28 Oct 2025ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Aermos
Generic Name
Electrocardiograph, professional, multichannel
Model / Reference
Aermos System
Primary DI / UDI-DI
00856298006411
510(k) Number
FDA Product Code
DRG, MWI, DRT
GMDN Term
Electrocardiograph, professional, multichannel
Device Class
Class II
Regulation Number
870.2910, 870.2300
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K250259)

Other devices from Scottcare Corporation, the

See all devices from Scottcare Corporation, the →

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