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MarginMap 304S

by Beekley Corporation

MarginMap 304S is a Class I device made by Beekley Corporation, listed in FDA GUDID since 22 Jul 2019 (UDI-DI 00815137021954), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00815137021954 UDI-DI Date22 Jul 2019ListedStatusListed 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  • Withdrawn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
MarginMap
Generic name
Radiographic image marker, manual
Model / reference
304S
Primary DI / UDI-DI
00815137021954
FDA product code
MJI
GMDN term
Radiographic image marker, manual
Device class
Class I
Regulation number
864.3010
GUDID distribution status
In Commercial Distribution

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Category: Radiographic image marker, manual

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Properties

  • Supplied sterile
  • Single use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)