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Pelimex ACT2230Express Dual

by Easywell Biomedicals, Inc.

Listed FDA GUDID listing, not in commercial distribution

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

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 Number10471765290474 UDI-DI Date20 Oct 2016ListedStatusListed GUDID: not in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Pelimex
Generic Name
Intermittent electronic patient thermometer
Model / Ref / Catalog
ACT2230Express Dual
Description
digital clinical thermometer+user manual Corrugated boxes Carton
Primary DI / UDI-DI
10471765290474
FDA Product Code
FLL
GMDN Term
Intermittent electronic patient thermometer
Device Class
Class II
Regulation Number
880.2910
GUDID distribution status
Not in Commercial Distribution

Other devices from Easywell Biomedicals, Inc.

Properties

  • Single Use
  • Over-the-Counter
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (9)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No