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Aermos Tx Patiet Cable 102205

by ScottCare Cardiovascular Solutions

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 Number00856298006442 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  • Withdrawn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 Tx Patiet Cable
Generic Name
Electrocardiograph, professional, single-channel
Model / Reference
102205
Primary DI / UDI-DI
00856298006442
510(k) Number
FDA Product Code
DRG, DRT, MWI
GMDN Term
Electrocardiograph, professional, single-channel
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 Cardiovascular Solutions

Properties

  • Prescription Use
  • Lot / Batch Number

Other properties (12)

  • 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
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No