3M™ Littmann® 8842
by 3M Company
3M™ Littmann® 8842 is a Class II device made by 3M Company, listed in FDA GUDID since 1 Jun 2023 (UDI-DI 00707387812669), 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 | Number00707387812669 | Date1 Jun 2023 | StatusListed |
Official records
- AccessGUDID record 00707387812669
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- 3M™ Littmann®
- Generic name
- Electronic acoustic stethoscope
- Model / Ref / Catalog
- 8842
- Primary DI / UDI-DI
- 00707387812669
- FDA product code
- DQD
- GMDN term
- Electronic acoustic stethoscope
- Device class
- Class II
- Regulation number
- 870.1875
- GUDID distribution status
- In Commercial Distribution
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