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BodyMed BDMCSBS10SAM

by Boxout, LLC

BodyMed BDMCSBS10SAM is a Class I device made by Boxout, LLC, listed in FDA GUDID since 5 Dec 2022 (UDI-DI 00815991024849), 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 Number00815991024849 UDI-DI Date5 Dec 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  • Withdrawn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
BodyMed
Generic name
Manual scalpel blade, single-use
Model / reference
BDMCSBS10SAM
Primary DI / UDI-DI
00815991024849
FDA product code
GFA
GMDN term
Manual scalpel blade, single-use
Device class
Class I
Regulation number
878.4820
GUDID distribution status
In Commercial Distribution

Related devices

Category: Manual scalpel blade, single-use

Similar devices in this category

Other devices filed under Manual scalpel blade, single-use.

Other devices from Boxout, LLC

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Properties

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