Breg Pad M/U Xl Ls Wo
by Breg, Inc.
Breg Pad M/U Xl Ls Wo (04740) is a Class II device made by Breg, Inc., listed in FDA GUDID since 15 Aug 2016 (UDI-DI 00672736001103), registry data as of 22 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 | Number00672736001103 | Date15 Aug 2016 | StatusListed |
Official records
- AccessGUDID record 00672736001103
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Breg
- Generic name
- Circulating-fluid localized thermal therapy system pack, single-use
- Model / Ref / Catalog
- PAD M/U XL LS WO, 04740
- Primary DI / UDI-DI
- 00672736001103
- FDA product code
- ILO
- GMDN term
- Circulating-fluid localized thermal therapy system pack, single-use
- Device class
- Class II
- Regulation number
- 890.5720
- GUDID distribution status
- In Commercial Distribution
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