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InfiMed Nexus, RF/DR, Non Varian Digital Receptor Nexus DRF (RF/DR)

by Infimed, 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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00858086006023 UDI-DI Date16 Sep 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  • Withdrawn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
InfiMed Nexus, RF/DR, Non Varian Digital Receptor
Generic Name
X-ray system computer, diagnostic, general-purpose
Model / Reference
Nexus DRF (RF/DR)
Primary DI / UDI-DI
00858086006023
FDA Product Code
MQB, JAA, OWB
GMDN Term
X-ray system computer, diagnostic, general-purpose
Device Class
Class II
Regulation Number
892.1680, 892.1650
GUDID distribution status
Not in Commercial Distribution

Other devices from Infimed, Inc.

See all devices from Infimed, Inc. →

Properties

  • Serial Number
  • Manufacturing Date

Other properties (12)

  • 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
  • Premarket Exempt: No
  • Lot / Batch Number: No
  • Expiration Date: No