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F112 RSSF112-7XF

by Burlington Medical, LLC

F112 RSSF112-7XF is a Class I device made by Burlington Medical, LLC, listed in FDA GUDID since 7 Oct 2022 (UDI-DI 00840331200959), 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 Number00840331200959 UDI-DI Date7 Oct 2022ListedStatusListed 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  • Withdrawn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
F112
Generic name
Radiation shielding apron
Model / reference
RSSF112-7XF
Primary DI / UDI-DI
00840331200959
FDA product code
IWO
GMDN term
Radiation shielding apron
Device class
Class I
Regulation number
892.6500
GUDID distribution status
In Commercial Distribution
MRI safety
MR Unsafe

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)