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EDM3 BP35

by Edm 3, LLC

EDM3 BP35 is a Class I device made by Edm 3, LLC, listed in FDA GUDID since 16 Sep 2022 (UDI-DI M202BP351), 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 NumberM202BP351 UDI-DI Date16 Sep 2022ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
EDM3
Generic name
Skin-coring punch, single-use
Model / Ref / Catalog
BP35
Primary DI / UDI-DI
M202BP351
FDA product code
MDM
GMDN term
Skin-coring punch, single-use
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution

Related devices

Category: Skin-coring punch, single-use

Similar devices

Other devices filed under FDA product code MDM (Instrument, Manual, Surgical, General Use).

Other devices from Edm 3, LLC

See all devices from Edm 3, LLC →

Properties

  • Supplied sterile
  • Single use
Other properties (13, all answered No)