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Sb-60-333

by Source-Ray, Inc.

Sb-60-333 (900046) is a Class I device made by Source-Ray, Inc., listed in FDA GUDID since 9 Sep 2016 (UDI-DI 00868162000203), registry data as of 21 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 21 Oct 2026.

Regulatory status

as of registry sync 21 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00868162000203 UDI-DI Date9 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  • Withdrawn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
X-ray tube housing assembly, diagnostic
Model / Ref / Catalog
SB-60-333, 900046
Primary DI / UDI-DI
00868162000203
FDA product code
ITY
GMDN term
X-ray tube housing assembly, diagnostic
Device class
Class I
Regulation number
892.1760
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code ITY (Assembly, Tube Housing, X-Ray, Diagnostic).

Other devices from Source-Ray, Inc.

  • Sr-115-Cg

    Class II
  • Sr-130-G

    Class II
  • Xrs-140-7.5K-P

    Class I
  • Rc-115

    Class II

See all devices from Source-Ray, Inc. →

Properties

  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)