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FEops 1.4.1

by FEops GUDID

Withdrawn United States

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number05430002070032 UDI-DIDate30 Nov 2021ListedStatusWithdrawn

Coverage

1 jurisdiction

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  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 23 Oct 2026.

Specification

GUDID

Trade Name
FEops
Generic Name
Radiology DICOM image processing application software
Model / Reference
1.4.1
Primary DI / UDI-DI
05430002070032
FDA Product Code
QQI
GMDN Term
Radiology DICOM image processing application software
Device Class
Class II
Regulation Number
870.1405
Commercial Distribution
Not in Commercial Distribution

Properties

  • Premarket Exempt

Other properties (13)

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