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Fvest RLFVEST8XLF

by Burlington Medical, LLC

Fvest RLFVEST8XLF is a Class I device made by Burlington Medical, LLC, listed in FDA GUDID since 12 Mar 2021 (UDI-DI 00840186656918), 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 Number00840186656918 UDI-DI Date12 Mar 2021ListedStatusListed 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  • Withdrawn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
Fvest
Generic name
Radiation shielding apron
Model / reference
RLFVEST8XLF
Primary DI / UDI-DI
00840186656918
FDA product code
EAJ
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)