Stethoscope 122-BLK
Stethoscope 122-BLK is a Class I device made by Rashman Corp., listed in FDA GUDID since 5 Dec 2022 (UDI-DI 00786511621223), 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 | Number00786511621223 | Date5 Dec 2022 | StatusListed |
Official records
- AccessGUDID record 00786511621223
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Stethoscope
- Generic name
- Mechanical external stethoscope
- Model / reference
- 122-BLK
- Primary DI / UDI-DI
- 00786511621223
- FDA product code
- LDE
- GMDN term
- Mechanical external stethoscope
- Device class
- Class I
- Regulation number
- 870.1875
- GUDID distribution status
- In Commercial Distribution
Similar devices
Other devices filed under FDA product code LDE (Stethoscope, Manual).
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- 3M™ Littmann® 2454 by 3M COMPANY
- GAMMA 3.2 000 M-000.09.942 by Heine Optotechnik GmbH & Co. KG
- VARIOUS TYPES OF STETHOSCOPES by Liaoning-Usa Corp.
- THE BLOOM STETHOSCOPE by Stethophonics, Inc.