Reusable Cordless Transducer TD-410
by Olympus Medical Systems Corporation FDA registration: Japan GUDID
Product code GEI
Regulatory status
Recall ongoing. 4 ongoing FDA recalls. See recalls
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number04953170421815 | Date4 Dec 2025 | StatusIn distribution |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not known
- Not covered
United States — GUDID listing Listed
Recalls
-
- Ongoing Z-1854-2026
- Ongoing Z-1851-2026
- Ongoing Z-1853-2026
- Ongoing Z-1852-2026
Potential for detachment of a distal tip component of the device during use.
Specification
- Trade Name
- Reusable Cordless Transducer
- Generic Name
- Ultrasonic surgical system transducer
- Model / Ref / Catalog
- TD-410, N6132940
- Primary DI / UDI-DI
- 04953170421815
- 510(k) Number
- FDA Product Code
- GEI, LFL
- GMDN Term
- Ultrasonic surgical system transducer
- Device Class
- Class II
- Regulation Number
- 878.4400
- Commercial Distribution
- In Commercial Distribution
- Sterilization Method
- Moist Heat or Steam Sterilization
Other devices from Olympus Medical Systems Corporation
Properties & raw data
Show properties, registry sources and raw records
Other properties (11)
- Sterile: No
- Single Use: No
- Implantable: No
- Contains Latex: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Premarket Exempt: No
- Lot / Batch Number: No
- Expiration Date: No
Sources (1)
- FDA UDI 5914a02f-b1fc-4abb-a30b-62e794c490d8