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K303 REK303-3XM

by Burlington Medical, LLC

K303 REK303-3XM is a Class I device made by Burlington Medical, LLC, listed in FDA GUDID since 9 Feb 2023 (UDI-DI 00197513003342), 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 Number00197513003342 UDI-DI Date9 Feb 2023ListedStatusListed 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  • Withdrawn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
K303
Generic name
Radiation shielding apron
Model / reference
REK303-3XM
Primary DI / UDI-DI
00197513003342
FDA product code
IWO
GMDN term
Radiation shielding apron
Device class
Class I
Regulation number
892.6500
GUDID distribution status
In Commercial Distribution

Related devices

Category: Radiation shielding apron

Other devices from Burlington Medical, LLC

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Properties

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