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601 UE601XXLF

by Burlington Medical, LLC

601 UE601XXLF is a Class I device made by Burlington Medical, LLC, listed in FDA GUDID since 23 Nov 2020 (UDI-DI 00840186601505), 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 Number00840186601505 UDI-DI Date23 Nov 2020ListedStatusListed 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  • Withdrawn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
601
Generic name
Radiation shielding apron
Model / reference
UE601XXLF
Primary DI / UDI-DI
00840186601505
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)