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BodyMed BDMARW50

by Boxout, LLC

BodyMed BDMARW50 is a Class I device made by Boxout, LLC, listed in FDA GUDID since 17 Feb 2023 (UDI-DI 00815991024771), 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 Number00815991024771 UDI-DI Date17 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  • Withdrawn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
BodyMed
Generic name
Patient medical adhesive remover
Model / reference
BDMARW50
Primary DI / UDI-DI
00815991024771
FDA product code
KOX
GMDN term
Patient medical adhesive remover
Device class
Class I
Regulation number
878.4730
GUDID distribution status
In Commercial Distribution

Related devices

Category: Patient medical adhesive remover

Similar devices in this category

Other devices filed under Patient medical adhesive remover.

Other devices from Boxout, LLC

See all devices from Boxout, LLC →

Properties

  • Supplied sterile
  • Single use
  • Premarket exempt
  • Lot / batch number
  • Serial number
  • Expiration date
  • Manufacturing date
Other properties (8, all answered No)