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Dunlee CTR2280

by Dunlee Corporation GUDID

Withdrawn United States

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00884838086258 UDI-DIDate16 May 2017ListedStatusWithdrawn

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  • Withdrawn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
Dunlee
Generic Name
X-ray tube housing assembly, diagnostic
Model / Ref / Catalog
CTR2280, 4598-013-14351
Primary DI / UDI-DI
00884838086258
FDA Product Code
ITY
GMDN Term
X-ray tube housing assembly, diagnostic
Device Class
Class I
Regulation Number
892.1760
Commercial Distribution
Not in Commercial Distribution

Properties

  • Premarket Exempt
  • Serial Number
  • Manufacturing Date

Other properties (11)

  • 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
  • Expiration Date: No