EDM3 BP60
by Edm 3, LLC
EDM3 BP60 is a Class I device made by Edm 3, LLC, listed in FDA GUDID since 15 Sep 2022 (UDI-DI M202BP601), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | NumberM202BP601 | Date15 Sep 2022 | StatusListed |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- EDM3
- Generic name
- Skin-coring punch, single-use
- Model / Ref / Catalog
- BP60
- Primary DI / UDI-DI
- M202BP601
- 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
Similar devices
Other devices filed under FDA product code MDM (Instrument, Manual, Surgical, General Use).
- LSSS RM04053 by Lockdown Medical Ltd
- CrossFT CFK-T475 by Conmed Corporation
- FENTEX 325312FX by FENTEX medical GmbH
- FENTEX 316300FX by FENTEX medical GmbH
- BOBsnare Device 082000 by LSI Solutions, Inc.
- Fistula Brush Proctology 200.62 by Ovesco Endoscopy AG
- AMERICAN BIOMED, INC. MICROSURGICAL INSTRUMENTS by American Biomaterials Corp.
- Vanguard® Microplasty® 32-485020 by Biomet Orthopedics, Inc.
- TUNNELER by Denver Biomedicals, Inc.
- Bending cylinder for Pectus bars, 13.7 mm supplement for 020-00021 020-00029 by MedXpert GmbH