3M™ Littmann® 6232
by 3M Company
3M™ Littmann® 6232 is a Class I device made by 3M Company, listed in FDA GUDID since 1 May 2023 (UDI-DI 00707387812003), 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 | Number00707387812003 | Date1 May 2023 | StatusListed |
Official records
- AccessGUDID record 00707387812003
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- 3M™ Littmann®
- Generic name
- Mechanical external stethoscope
- Model / Ref / Catalog
- 6232
- Primary DI / UDI-DI
- 00707387812003
- FDA product code
- LDE
- GMDN term
- Mechanical external stethoscope
- Device class
- Class I
- Regulation number
- 870.1875
- GUDID distribution status
- In Commercial Distribution