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EPIQ Elite Diagnostic Ultrasound System 989606706051

by Philips Ultrasound LLC

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

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 Number00884838099111 UDI-DI Date10 Mar 2020ListedStatusListed GUDID: 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  • Withdrawn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
EPIQ Elite Diagnostic Ultrasound System
Generic Name
General-purpose ultrasound imaging system
Model / Reference
989606706051
Primary DI / UDI-DI
00884838099111
FDA Product Code
IYN
GMDN Term
General-purpose ultrasound imaging system
Device Class
Class II
Regulation Number
892.1550
GUDID distribution status
In Commercial Distribution

Related devices

Category: General-purpose ultrasound imaging system

Other devices from Philips Ultrasound LLC

See all devices from Philips Ultrasound LLC →

Properties

  • Prescription Use
  • Serial 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
  • Lot / Batch Number: No
  • Expiration Date: No
  • Manufacturing Date: No