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RapidCHECK RC1000

by Sun Nuclear Corporation 2 variants

RapidCHECK RC1000 is a Class I device made by Sun Nuclear Corporation, listed in FDA GUDID since 10 May 2026 (UDI-DI 05060608881499), registry data as of 23 Oct 2026.

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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number05060608881499 UDI-DI Date10 May 2026ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
RapidCHECK
Generic name
Multidisciplinary medical image management software
Model / reference
RC1000
Primary DI / UDI-DI
05060608881499
FDA product code
LHO
GMDN term
Multidisciplinary medical image management software
Device class
Class I
Regulation number
892.1940
GUDID distribution status
In Commercial Distribution

Other devices from Sun Nuclear Corporation

See all devices from Sun Nuclear Corporation →

Properties

  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (11, all answered No)