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Cs 8100 3D

by Carestream Health, Inc. 3 variants

Cs 8100 3D (5311162) is a Class II device made by Carestream Health, Inc., listed in FDA GUDID since 16 Sep 2016 (UDI-DI 60889975311166), registry data as of 8 Jun 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 8 Jun 2026.

Regulatory status

as of registry sync 8 Jun 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number60889975311166 UDI-DI Date16 Sep 2016ListedStatusListed 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  • Withdrawn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

Generic name
Stationary extraoral dental x-ray system, digital
Model / Ref / Catalog
CS 8100 3D, 5311162
Primary DI / UDI-DI
60889975311166
FDA product code
MUH, OAS
GMDN term
Stationary extraoral dental x-ray system, digital
Device class
Class II
Regulation number
872.1800, 892.1750
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code MUH (System,x-ray,extraoral source,digital).

Other devices from Carestream Health, Inc.

See all devices from Carestream Health, Inc. →

Properties

  • Prescription use
  • Serial number
Other properties (13, all answered No)